Welch Allyn, Inc.
Welch Allyn, Inc. holds FDA 510(k) medical device clearances, first cleared 1977, most recent 2025, with 5 FDA device recalls on record.
Clearances by Welch Allyn, Inc. — page 2
101–111 of 111- K771864 — WALL TRANSFORMERS 74710 & 74910
- K771900 — 71110 DESK CHARGER
- K771481 — TONGUE BLADE HOLDER
- K771181 — VAGINAL ILLUMINATOR, MODEL 78570
- K770906 — ANOSCOPE, OPTIC, FIBER
- K770768 — OPHTHALMOSCOPE, MODEL #11100
- K770769 — OTOSCOPE/ILLUMINATOR, MODEL #21100
- K770770 — WALL CHARGER, MODEL #79111
- K770291 — SIGMOIDOSCOPE, DISPOSABLE, MODEL #53125
- K770053 — MIRROR, LARYNGEAL
- K770054 — MIRROR, NASO-PHARYNX
Data sourced from openFDA. This site is unofficial and independent of the FDA.