FDA Device Intelligence
Home › BRIDON, CORP. › BContak

BContak

BRIDON, CORP. · Model B1332 · UDI-DI 00850023087997

KGM
0
510(k) clearances
20
Adverse events
0
Recalls
0
Facilities

Description

Skin Closure Adhesive Srip 1/2 x 4 CS

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.