FDA Device Intelligence
Home › WELCH ALLYN, INC. › Welch Allyn, Inc.

Welch Allyn, Inc.

WELCH ALLYN, INC. · Model 901075 · UDI-DI 00732094079692

FER Prescription
1
510(k) clearances
86
Adverse events
1
Recalls
46
Facilities

Description

Welch Allyn Rigid Operating Anoscope with Obturator; Light Carrier Not Included; 19 mm x 8.9 cm

Recalls

DateFirmReason
2018-12-12Applied Medical Resources CorpUnintentional shifting of the tip insulation of the firm's electrosurgical probes.

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.