FDA applicant

Sol Weiss MD, Inc.

Reseda, CA3 decisions2001–20020 recalls

FDA records 3 decisions for Sol Weiss MD, Inc. (Reseda, CA) from 2001 to 2002: 3 510(k) clearances. All are in product code HIB (Speculum, Vaginal, Nonmetal). 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, obstetrics and gynecology panel, where it files most

How often FDA has decided Sol Weiss MD, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Sol Weiss MD, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Sol Weiss MD, 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

Sol Weiss MD, Inc.

Which product codes does it file in?

What has FDA decided for it lately?