FDA Device Intelligence
Home › TECO DIAGNOSTICS › TECO DIAGNOSTICS

TECO DIAGNOSTICS

TECO DIAGNOSTICS · Model RPR-500 · UDI-DI 10673486000696

GMQ Prescription
1
510(k) clearances
37
Adverse events
0
Recalls
17
Facilities

Description

RPR, 1x500 Tests

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.