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

BR Surgical, LLC

BR Surgical, LLC · Model BR44-24609 · UDI-DI 00840183500504

KAE
10
510(k) clearances
82
Adverse events
1
Recalls
225
Facilities

Description

HARTMAN Ear Forcep, 1.5mm x 4mm, extra delicate, working length 2 3/8", overall 5 1/8"

Recalls

DateFirmReason
2025-01-31Aesculap IncThe forceps have been used in ways not covered by the design resulting in breakage of the clamps.

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.