FDA applicant

Stiefel Research Institute, Inc.

Oakhill, NY6 decisions1989–19920 recalls

FDA records 6 decisions for Stiefel Research Institute, Inc. (Oakhill, NY) from 1989 to 1992: 6 510(k) clearances. Most are in product codes GEH (Unit, Cryosurgical, Accessories) and IYO (System, Imaging, Pulsed Echo, Ultrasonic). 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 Stiefel Research Institute, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Stiefel Research Institute, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Stiefel”

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

Stiefel Laboratories, Inc. 1

Stiefel Research Institute, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Stiefel”