510(k) Report

FDA applicant

Implantology Corp.

Pine Brook, NJ9 decisions1993–19940 recalls

FDA records 9 decisions for Implantology Corp. (Pine Brook, NJ) from 1993 to 1994: 9 510(k) clearances. Most are in product codes JDG (Prosthesis, Hip, Femoral Component, Cemented…) and JDL (Prosthesis, Hip, Semi-Constrained (Metal…). 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 Implantology Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Implantology Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Implantology Corp.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report