FDA applicant

Osteoimplant Technology, Inc.

Hunt Valley, MD21 decisions1996–200511 recalls

FDA records 21 decisions for Osteoimplant Technology, Inc. (Hunt Valley, MD) from 1996 to 2005: 21 510(k) clearances. Most are in product codes LPH (Prosthesis, Hip, Semi-Constrained…) and JDI (Prosthesis, Hip, Semi-Constrained…). 11 recalls are 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 Osteoimplant Technology, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Osteoimplant Technology, Inc. since 2007.

Recalls per year

1in 2008

2007high 10 (2007) · low 0 (2009)2026

Class I Class II/III not classified

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

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Osteoimplant Technology, Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

What has been recalled?