FDA Device Intelligence
Home › Medtech Products Inc. › Nix

Nix

Medtech Products Inc. · Model 10363736110069 · UDI-DI 00363736110062

LIL
10
510(k) clearances
0
Adverse events
0
Recalls
2
Facilities

Description

Nix Ultra Removal Kit 12

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.