FDA applicant

Charles L. Rose and Co., Inc.

Mountain View, CA4 decisions1990–19920 recalls

FDA records 4 decisions for Charles L. Rose and Co., Inc. (Mountain View, CA) from 1990 to 1992: 4 510(k) clearances. Most are in product codes GEX (Powered Laser Surgical Instrument) and HGF (Source, Abortion Unit, Vacuum). 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 and plastic surgery panel, where it files most

How often FDA has decided Charles L. Rose and Co., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Charles L. Rose and Co., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Charles L. Rose and Co., 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 “Charles”

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

Charles A. Smith 2 Charles Polo & Co., Inc. 2 Charles Atkins & Co. 2 Charles I. Rose & Co., Inc. 1 Charles F. Samelson, M.D. 1 Charles D. Bell, Inc. 1 Charles Scharf 1

Charles L. Rose and Co., Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Charles”