FDA applicant

Firstar Healthcare Company Limited (Guangzhou)

Guangzhou, CN1 decision2020–20200 recalls

FDA records 1 decision for Firstar Healthcare Company Limited (Guangzhou) (Guangzhou, CN) in 2020: 1 510(k) clearance. All are in product code CBP (Valve, Non-Rebreathing). 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, anesthesiology panel, where it files most

How often FDA has decided Firstar Healthcare Company Limited (Guangzhou)’s devices, and how often a recall has named them.

FDA decisions per year

1in 2020

2020high 1 (2020) · low 0 (2021)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2020.

FIG. 1 — Firstar Healthcare Company Limited (Guangzhou) by year, 2020–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Firstar Healthcare Company Limited…’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 “Firstar”

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

Firstar Dental Company 1 Firstar Healthcare Co., Ltd. 1

Firstar Healthcare Company Limited (Guangzhou)

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Firstar”