{"uid":"cap_2M_-vj6jafDptuzlYEhZ_","slug":"medapi-medical-devices-endpoint-bcb61873","name":"MedAPI Medical Devices Endpoint","description":"Drug data, adverse events, clinical trials, PubMed. AI-powered medical analysis. 17 endpoints. x402 on Base.","url":"https://mamujamedapi.vercel.app/api/devices","method":"POST","headers":{},"bodySchema":null,"responseSchema":null,"example":null,"exampleRequest":null,"tags":["x402"],"displayCostAmount":"0.2","displayCostAsset":"USDC","priceDynamic":false,"priceHint":null,"priceStatus":"priced","priceSource":"registry","requiresHandshake":false,"reviewCount":0,"rating":{"score":"0.00","successRate":"0.00","reviews":0,"stars":null,"state":"unrated"},"availabilityStatus":"unknown","priceObserved":null,"sessionDeposit":null,"pricing":{"kind":"static","summary":"$0.2/call","primary":{"kind":"static","protocol":"x402","network":"base","amountUsd":"0.2","per":"call","confidence":"exact"},"accepted":[{"kind":"static","protocol":"x402","network":"base","amountUsd":"0.2","per":"call","confidence":"exact"}]},"paymentMethods":[{"uid":"pm_znX5Na7TEtEQWZQVXwmUN","protocol":"x402","methodType":"crypto","chain":"base","mode":"charge","costAmount":"0.2","costPer":"request","priority":0,"asset":null,"unit":"request","depositMicros":null,"planRef":null}],"brandName":null,"brandSlug":null,"brandBaseUrl":null,"brandDocsUrl":null,"whatItDoes":"Searches and retrieves FDA medical device data, recalls, and adverse event reports for a specified device or query","exampleAgentPrompt":"Can you search the FDA medical device database for adverse event reports and recall information on the Philips DreamStation CPAP machine?","exampleUseCases":[{"title":"Medical device recall safety check","prompt":"I need to know if the insulin pump I was prescribed has any FDA recalls or safety alerts — can you look up adverse events and recall status for the Medtronic MiniMed 670G?"},{"title":"Device regulatory classification research","prompt":"What is the FDA classification and regulatory status for continuous glucose monitors? I need to know if there are any flagged safety issues or recent adverse event reports."},{"title":"Manufacturer device safety audit","prompt":"Pull all FDA adverse event records and recall notices for medical devices made by Boston Scientific so I can review their safety history."}],"resultDescription":"Returns structured data about medical devices including FDA classification, recall status, adverse event reports, manufacturer details, device type, regulatory clearance information, and safety alerts as sourced from FDA databases.","failureModes":["Device not found in FDA database returns empty results","Ambiguous device name may return unrelated results","FDA database may have incomplete or delayed adverse event records","Malformed or missing query parameters return 400 error","Service unavailability or timeout from upstream FDA data source","Payment failure on x402 protocol returns 402 error"],"whenToPreferThis":"Use this endpoint when you need authoritative FDA data specifically about medical devices — recalls, adverse events, classification, or manufacturer information. Prefer this over general web search when you need structured, queryable regulatory data about physical medical equipment rather than drugs or clinical trials.","instructions":null,"reviewSummary":null,"reviewSummaryHighlights":null,"reviewSummaryConcerns":null,"reviewSummaryGeneratedAt":null,"activationCount":0,"lastUsedAt":null,"lastSuccessfullyRanAt":null,"lastHealthCheckAt":"2026-09-14T06:35:18.462Z","isFirstParty":false}