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

BR Surgical, LLC

BR Surgical, LLC · Model BR48-28679 · UDI-DI 00840183523633

KBN
3
510(k) clearances
47
Adverse events
1
Recalls
212
Facilities

Description

Silicone Pads for CROWE-DAVIS Mouth Gag Frame (2 each)

Recalls

DateFirmReason
2018-02-16Aesculap Implant Systems LLCThe plastic sleeves of the Penis Clamp and Mouth Gag may stick together during or after reprocessing rendering the instruments unusable.

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.