Home › Device types › FPX

Strip, Adhesive, Closure, Skin

FDA product code FPX · Class 1 · General Hospital

105

Registered devices

64

Adverse events

1

Recalls

35

510(k) clearances

Devices with this code

Sterion® Skin Closure — ASPEN SURGICAL PRODUCTS, INC.Henry Schein — HENRY SCHEIN, INC.Sterion® Skin Closure — ASPEN SURGICAL PRODUCTS, INC.Sterion® Skin Closure — ASPEN SURGICAL PRODUCTS, INC.Sterion® Skin Closure — ASPEN SURGICAL PRODUCTS, INC.Sterion® Skin Closure — ASPEN SURGICAL PRODUCTS, INC.Sterion® Skin Closure — ASPEN SURGICAL PRODUCTS, INC.Sterion® Skin Closure — ASPEN SURGICAL PRODUCTS, INC.ACE — ACE SURGICAL SUPPLY CO., INC.Sterion® Skin Closure — ASPEN SURGICAL PRODUCTS, INC.Sterion® Skin Closure — ASPEN SURGICAL PRODUCTS, INC.Shur Strip® — Derma Sciences Canada Inc Suture Strip® — Derma Sciences Canada Inc Dukal — Dukal LLC Sterion® Skin Closure — ASPEN SURGICAL PRODUCTS, INC.Suture Strip® — Derma Sciences Canada Inc Henry Schein — HENRY SCHEIN, INC.Sterion® Skin Closure — ASPEN SURGICAL PRODUCTS, INC.Sterion® Skin Closure — ASPEN SURGICAL PRODUCTS, INC.CARDINAL HEALTH — Cardinal Health 200, LLC Shur-Strip® — Derma Sciences Canada Inc Sterion® Skin Closure — ASPEN SURGICAL PRODUCTS, INC.Aspen® Skin Closure — ASPEN SURGICAL PRODUCTS, INC.Sterion® Skin Closure — ASPEN SURGICAL PRODUCTS, INC.

Recent recalls

Date	Firm	Reason
2013-07-18	Aspen Surgical Products, Inc.	Aspen Surgical is recalling Wound Closures because firm could not confirm sterility, after FDA sampling indicated the product may not be sterile. Using the reca

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API key Read the docs

Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.