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Welch Allyn, Inc.

WELCH ALLYN, INC. · Model 901075 · UDI-DI 00732094080902

KDM Prescription
1
510(k) clearances
0
Adverse events
1
Recalls
1
Facilities

Description

Welch Allyn Rigid Fiber-Optic Sigmoidoscope with Obturator; 11 mm x 25 cm

Recalls

DateFirmReason
2021-04-23Adler MicroMed, Inc.Due to issue with product sterility. Sterilization service provider had falsified records.

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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.