FDA applicant

Self Sharpening Surgical Steel, Inc.

Detroit, MI1 decision1986–19860 recalls

FDA records 1 decision for Self Sharpening Surgical Steel, Inc. (Detroit, MI) in 1986: 1 510(k) clearance. All are in product code GEI (Electrosurgical, Cutting & Coagulation &…). 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 Self Sharpening Surgical Steel, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Self Sharpening Surgical Steel, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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See the 510(k) Report

Other applicant names beginning “Self”

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

Self Regulation Systems, Inc. 3 Self Care Systems, Inc. 3 Self Doctor Care, LLC 1

Self Sharpening Surgical Steel, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Self”