FDA Device Intelligence
HomeBR Surgical, LLC › BR Surgical, LLC

BR Surgical, LLC

BR Surgical, LLC · Model BR74-50218 · UDI-DI 00840183524784

GAF
5
510(k) clearances
10
Adverse events
1
Recalls
205
Facilities

Description

Cement Mixing Spatula, double ended, 7 1/4"

Recalls

DateFirmReason
2024-12-03Sklar InstrumentsReports of various packaging issues that may result in a breach of the sterile barrier.

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.