MTI
Medical Technology Industries, Inc. · Model 130-1770-00-238 · UDI-DI 10840118420751
0
510(k) clearances
3
Adverse events
0
Recalls
40
Facilities
Description
Procedure Table, Hand/Forearm G2 PREMIUM-BURGUNDY
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 docsData 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.