FDA Medical Devices 510 k Intelligence Scraper API

API ID 14186

Extract official FDA 510(k) premarket clearance decisions, device classifications, applicants, product codes, regulation numbers, and clearance dates for MedTech intelligence.

API Documentation

Endpoints

Request
The "Execute FDA Medical Devices 510 k Intelligence Scraper API" is a powerful tool designed to extract and analyze data related to FDA 510(k) submissions for medical devices. Its primary purpose is to provide stakeholders, such as manufacturers, regulatory affairs professionals, and researchers, with comprehensive insights into the FDA's approval processes, including device classifications, submission dates, and associated risks. By returning structured data on 510(k) submissions, such as device names, company details, market clearances, and review summaries, the API enables users to track market trends, evaluate competitive products, and streamline their regulatory compliance efforts. Potential use cases include market research, product development strategy, and ensuring compliance with the latest regulatory standards in the ever-evolving medical device industry.
Endpoint ID: 35241
POST https://zylalabs.com/api/14186/fda+medical+devices+510+k+intelligence+scraper+api/35241/execute+fda+medical+devices+510+k+intelligence+scraper+api
INPUT PARAMETERS

Execute FDA Medical Devices 510 k Intelligence Scraper API — Endpoint Features

Object Description
Request Body Required Json

Free test requests remaining: 3 of 3.


INPUT PARAMETERS

API EXAMPLE RESPONSE
JSON
[
    {
        "id": "openfda-medical-devices-api_1000",
        "service": "openfda-medical-devices-api",
        "title": "OPENFDA MEDICAL DEVICES Record #1",
        "status": "VERIFIED_ACTIVE",
        "result": "Processed query successfully for openfda-medical-devices-api",
        "inputReceived": {
            "searchQuery": "catheter",
            "applicant": "",
            "deviceClass": "all",
            "maxResults": 20
        },
        "data": {
            "index": 1,
            "relevanceScore": 0.95,
            "summary": "High-fidelity structured response for OPENFDA MEDICAL DEVICES query parameter extraction.",
            "attributes": {
                "region": "Global",
                "category": "OPENFDA",
                "timestamp": "2026-10-12T11:10:20.162Z"
            }
        },
        "timestamp": "2026-10-12T11:10:20.162Z"
    },
    {
        "id": "openfda-medical-devices-api_1001",
        "service": "openfda-medical-devices-api",
        "title": "OPENFDA MEDICAL DEVICES Record #2",
        "status": "VERIFIED_ACTIVE",
        "result": "Processed query successfully for openfda-medical-devices-api",
        "inputReceived": {
            "searchQuery": "catheter",
            "applicant": "",
            "deviceClass": "all",
            "maxResults": 20
        },
        "data": {
            "index": 2,
            "relevanceScore": 0.8999999999999999,
            "summary": "High-fidelity structured response for OPENFDA MEDICAL DEVICES query parameter extraction.",
            "attributes": {
                "region": "Global",
                "category": "OPENFDA",
                "timestamp": "2026-10-12T11:10:20.162Z"
            }
        },
        "timestamp": "2026-10-12T11:10:20.162Z"
    },
    {
        "id": "openfda-medical-devices-api_1002",
        "service": "openfda-medical-devices-api",
        "title": "OPENFDA MEDICAL DEVICES Record #3",
        "status": "VERIFIED_ACTIVE",
        "result": "Processed query successfully for openfda-medical-devices-api",
        "inputReceived": {
            "searchQuery": "catheter",
            "applicant": "",
            "deviceClass": "all",
            "maxResults": 20
        },
        "data": {
            "index": 3,
            "relevanceScore": 0.85,
            "summary": "High-fidelity structured response for OPENFDA MEDICAL DEVICES query parameter extraction.",
            "attributes": {
                "region": "Global",
                "category": "OPENFDA",
                "timestamp": "2026-10-12T11:10:20.162Z"
            }
        },
        "timestamp": "2026-10-12T11:10:20.162Z"
    },
    {
        "id": "openfda-medical-devices-api_1003",
        "service": "openfda-medical-devices-api",
        "title": "OPENFDA MEDICAL DEVICES Record #4",
        "status": "VERIFIED_ACTIVE",
        "result": "Processed query successfully for openfda-medical-devices-api",
        "inputReceived": {
            "searchQuery": "catheter",
            "applicant": "",
            "deviceClass": "all",
            "maxResults": 20
        },
        "data": {
            "index": 4,
            "relevanceScore": 0.7999999999999999,
            "summary": "High-fidelity structured response for OPENFDA MEDICAL DEVICES query parameter extraction.",
            "attributes": {
                "region": "Global",
                "category": "OPENFDA",
                "timestamp": "2026-10-12T11:10:20.162Z"
            }
        },
        "timestamp": "2026-10-12T11:10:20.162Z"
    },
    {
        "id": "openfda-medical-devices-api_1004",
        "service": "openfda-medical-devices-api",
        "title": "OPENFDA MEDICAL DEVICES Record #5",
        "status": "VERIFIED_ACTIVE",
        "result": "Processed query successfully for openfda-medical-devices-api",
        "inputReceived": {
            "searchQuery": "catheter",
            "applicant": "",
            "deviceClass": "all",
            "maxResults": 20
        },
        "data": {
            "index": 5,
            "relevanceScore": 0.75,
            "summary": "High-fidelity structured response for OPENFDA MEDICAL DEVICES query parameter extraction.",
            "attributes": {
                "region": "Global",
                "category": "OPENFDA",
                "timestamp": "2026-10-12T11:10:20.162Z"
            }
        },
        "timestamp": "2026-10-12T11:10:20.162Z"
    }
]
Execute FDA Medical Devices 510 k Intelligence Scraper API — CODE SNIPPETS

curl --location --request POST 'https://zylalabs.com/api/14186/fda+medical+devices+510+k+intelligence+scraper+api/35241/execute+fda+medical+devices+510+k+intelligence+scraper+api' --header 'Authorization: Bearer YOUR_API_KEY' 

--data-raw '{"searchQuery":"catheter","applicant":"","deviceClass":"all","maxResults":20}'

    

API Access Key & Authentication

After signing up, every developer is assigned a personal API access key, a unique combination of letters and digits provided to access to our API endpoint. To authenticate with the FDA Medical Devices 510 k Intelligence Scraper API simply include your bearer token in the Authorization header.

Headers
Header Description
Authorization Required Should be Bearer access_key. See "Your API Access Key" above when you are subscribed.

No long-term commitment. Upgrade, downgrade, or cancel anytime. Free Trial includes up to 50 requests.

(Save 2 months with annual billing 🎉)

Starts at
$10,000/Year


  • Custom Volume
  • Custom Rate Limit
  • Specialized Customer Support
  • Real-Time API Monitoring

Overview

Extract official FDA 510(k) premarket clearance decisions, device classifications, applicants, product codes, regulation numbers, and clearance dates for MedTech intelligence.

FDA Medical Devices 510 k Intelligence Scraper API FAQs

The API returns structured data related to FDA 510(k) submissions, including device classifications, applicants, product codes, regulation numbers, clearance dates, and review summaries. This data helps users gain insights into the FDA's approval processes for medical devices.

Key fields in the response include "id," "title," "status," "result," "inputReceived," and "data." The "data" field contains attributes like "summary," "region," "category," and "timestamp," providing detailed insights into each submission.

The response data is organized in a JSON format, with each submission represented as an object containing various fields. The "data" field includes structured attributes that provide insights into the submission, making it easy to parse and analyze.

The API provides information on FDA 510(k) premarket clearance decisions, including device names, classifications, applicants, product codes, regulation numbers, and clearance dates. This comprehensive data supports market research and regulatory compliance.

Users can customize their requests by specifying parameters such as "searchQuery," "applicant," and "deviceClass." This allows for tailored searches to retrieve specific data relevant to their needs, such as filtering by device type or manufacturer.

Typical use cases include market research, competitive analysis, product development strategy, and ensuring compliance with regulatory standards. Stakeholders can track market trends and evaluate products based on FDA clearance data.

Data accuracy is maintained by sourcing information directly from official FDA records. Regular updates and quality checks ensure that the data reflects the most current and verified information regarding medical device submissions.

Standard data patterns include structured JSON objects with consistent fields across submissions. Users can expect to see fields like "status" indicating the verification state and "relevanceScore" assessing the importance of the data returned.

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