510(k) Report

FDA applicant

Lhasa Medical, Inc.

Weymouth, MA11 decisions1996–20030 recalls

FDA records 11 decisions for Lhasa Medical, Inc. (Weymouth, MA) from 1996 to 2003: 11 510(k) clearances. Most are in product codes MQX (Needle, Acupuncture, Single Use) and ILY (Lamp, Infrared, Therapeutic Heating). Its devices cite 8 predicates, 3 of them its own earlier devices. No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, general hospital panel, where it files most

How often FDA has decided Lhasa Medical, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Lhasa Medical, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Lhasa Medical, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Lhasa Medical, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Other applicant names beginning “Lhasa”

FDA records each applicant name separately; these may or may not be the same firm.