FDA applicant

Procedure Products, Inc.

Vancouver, WA16 decisions1981–20171 recall

FDA records 16 decisions for Procedure Products, Inc. (Vancouver, WA) from 1981 to 2017: 16 510(k) clearances. Most are in product codes FMF (Syringe, Piston) and DQO (Catheter, Intravascular, Diagnostic). Its devices cite 1 predicate, 0 of them its own earlier devices. 1 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 Procedure Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2017

2007high 1 (2017) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

1in 2015

2007high 1 (2015) · low 0 (2007)2026

Class I Class II/III not classified

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

Planning a device like Procedure Products, 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 “Procedure”

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

Procedure Packs, Inc. 4 Procedure Pak, Inc. 2

Procedure Products, Inc.

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?

What has been recalled?

Other applicant names beginning “Procedure”