FDA Device Intelligence
Home › AESCULAP, INC. › AESCULAP

AESCULAP

AESCULAP, INC. · Model MA305R · UDI-DI 04046964566233

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

Description

DAVIS Mouth Gag, #2, 23 x 64 mm, non-sterile, reusable

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.