Home › Aesculap AG › AESCULAP
AESCULAP
Aesculap AG · Model OM071R · UDI-DI 04038653053285
KBN
Prescription
3
510(k) clearances
47
Adverse events
1
Recalls
212
Facilities
Description
WHITEHEAD-JENNINGS Mouth Gag, 4 1/4", (110 mm), non-sterile, reusable
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2018-02-16 | Aesculap Implant Systems LLC | The 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 docsData 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.