FDA Device Intelligence
Home3M UNITEK CORPORATION › 3M™ Unitek™

3M™ Unitek™

3M UNITEK CORPORATION · Model 160-373 · UDI-DI 00652221045232

ECM Prescription
2
510(k) clearances
4
Adverse events
0
Recalls
86
Facilities

Description

Unitek(TM) Molar Band General Purpose Wide Regular Temper U6,7 Size 36+ Ea

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.