FDA Device Intelligence
HomeWELCH ALLYN, INC. › Welch Allyn, Inc.

Welch Allyn, Inc.

WELCH ALLYN, INC. · Model 901027 · UDI-DI 00732094067828

HMF Prescription
10
510(k) clearances
19
Adverse events
0
Recalls
41
Facilities

Description

Welch Allyn 767 Integrated Wall Diagnostic System including Wall Aneroid Sphygmomanometer (#7670-01), Coaxial Ophthalmoscope (#11720), KleenSpec Disposable Specula Dispenser, Wall-Mount Panel (34 x 12 in / 86.4 x 30.5 cm); IEC Plug Type-B

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.