FDA applicant

Paul Weiser Co.

Los Angeles, CA1 decision1988–19880 recalls

FDA records 1 decision for Paul Weiser Co. (Los Angeles, CA) in 1988: 1 510(k) clearance. All are in product code ITI (Wheelchair, Powered). 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, physical medicine panel, where it files most

How often FDA has decided Paul Weiser Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Paul Weiser Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Paul”

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

Paul Hartmann Corp. 5 Paul B. Elder Co. 3 Paul B. Heller, D.M.D. 1 Paul E. Jaffe, D.M.D. 1 Paul H. Schneider Ent. 1 Paul Ritzau Pari GmbH 1 Paul S. Barclay, D.D.S., Ltd. 1 Paul Ritzau Pari-Werk GmbH 1

Paul Weiser Co.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Paul”