FDA applicant

Schoelly Technologies, Inc.

Hollywood, FL2 decisions1995–19950 recalls

FDA records 2 decisions for Schoelly Technologies, Inc. (Hollywood, FL) in 1995: 2 510(k) clearances. Most are in product codes HRX (Arthroscope) and GCJ (Laparoscope, General & Plastic Surgery). 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, orthopedic panel, where it files most

How often FDA has decided Schoelly Technologies, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Schoelly Technologies, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Schoelly Technologies, 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 “Schoelly”

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

Schoelly Fiberoptic GmbH 12 Schoelly Imaging, Inc. 5

Schoelly Technologies, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Schoelly”