Merge HRIS (BYOK)
Read employees, employments, time off, timesheets, groups and work locations from the HR system linked to your Merge account, with your own keys (no pay, ID or birth data)
Discover
OpenAPIRead your data6 tools
Open FDA Devices (BYOK)
Search FDA medical device 510(k) clearances, PMA approvals, product classifications, UDI records and establishment listings with your own openFDA key
Unify Dynamics LLC
Tools6read-only
Sign-inBYOKbring your own key
Key keptNeverused for one call only
PriceFreeoptional Pro limits
ProviderOpen FDA Devicesunofficial, not affiliated
Works withMCP · RESTany agent
Try asking
Real questions, and the tools your agent calls to answer them.
Which 510(k) clearances were decided for insulin pumps in 2025?
Tools called
search_device_510k_clearancesWhich PMA approvals exist for cochlear implants?
Tools called
search_device_pma_approvalsWhat class is a daily-wear contact lens?
Tools called
search_device_classificationsFind UDI records for the brand 'Accu-Chek'.
Tools called
search_device_udiWhich establishments list a product linked to 510(k) K123456?
Tools called
search_device_establishment_listingsHow many 510(k) submissions got each decision code?
Tools called
count_device_recordsAbout
Open FDA Devices (BYOK) lets an AI assistant read your own Open FDA Devices data through the Open FDA Devices API with a key you supply (openFDA API key). Read-only: 6 tools (search_device_510k_clearances, search_device_pma_approvals, search_device_classifications, search_device_udi, search_device_establishment_listings, count_device_records). The BYOK key travels with each request, is used for that one call only and is never stored, logged or cached; it is only ever sent to api.fda.gov. Unofficial connector by Unify Dynamics LLC: not affiliated with, endorsed by or sponsored by Open FDA Devices. Open FDA Devices and its logos are trademarks of their owners and are used only to say which service the connector works with.
Sources: Live from the Open FDA Devices API (api.fda.gov) with a BYOK key; documentation: https://open.fda.gov/apis/device/. Endpoints checked against that documentation on 2026-10-16.
Privacy
The publisher, Unify Dynamics LLC, states that tool inputs are processed in memory and not retained.
Data not collectedNo account, no profile, no stored prompts or results.
What it can do
6 tools, grouped by job. Every one is read-only or compute-only.
- Search device 510k clearancesSearch FDA 510(k) premarket notifications: K number, device name, applicant, decision and dates, product code, advisory committee, clearance type…
- Search device pma approvalsSearch FDA premarket approvals (PMA) and supplements: PMA number, supplement, trade and generic name, applicant, decision, dates, product code and…
- Search device classificationsSearch FDA device classifications by product code: device name, class (1, 2 or 3), regulation number, medical specialty, review panel and flags…
- Search device udiSearch the Global UDI database of device identifiers: brand, company, model and catalog number, description, distribution status, prescription…
- Search device establishment listingsSearch FDA device registration and listing records: proprietary names, establishment types, linked 510(k) and PMA numbers, listed products and…
- Count device recordsCount how often each value of a field occurs among matching records of one device dataset, for example 510(k) decisions by decision_code.
Information
PublisherUnify Dynamics LLC
CategoryHealth & care
LanguagesEnglish
Built forWorldwide
CompatibilityAny MCP client · any agent · REST
Version0.1.0
MCP endpoint
https://byok-openfda-devices.connectorbay.com/mcpREST APIopenapi.json
CountryWorldwide
FunctionOther
LayerDeep connectors
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