FDA applicant

Osteo-Technology Intl., Inc.

Timonium, MD3 decisions1993–19950 recalls

FDA records 3 decisions for Osteo-Technology Intl., Inc. (Timonium, MD) from 1993 to 1995: 3 510(k) clearances. Most are in product codes HRS (Plate, Fixation, Bone) and JDI (Prosthesis, Hip, Semi-Constrained…). 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 Osteo-Technology Intl., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Osteo-Technology Intl., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Osteo-Technology Intl., 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 “Osteo-Technology”

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

Osteo Technology, Inc. 18 Osteo AG 9 Osteo Implant Corp. 2 Osteo Vasive, LLC 1

Osteo-Technology Intl., Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Osteo-Technology”