FDA Device Intelligence
Home › VAN SICKLE SURGICAL INSTRUMENTS, INCORPORATED › Van Sickle

Van Sickle

VAN SICKLE SURGICAL INSTRUMENTS, INCORPORATED · Model 32-205 · UDI-DI 00810207783695

KAE
10
510(k) clearances
89
Adverse events
1
Recalls
226
Facilities

Description

Lempert Rongeur 6-1/4" (158 mm) curved, delicate, 2.5mm wide bite

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.