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MOUTH GAG

KLS-Martin L.P. · Model 96-256-34-07 · UDI-DI 00888118090164

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

Description

CHILDRENS HOSPITAL

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.

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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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.