FDA applicant

Titan Implants

Flemington, NJ4 decisions2001–20050 recalls

FDA records 4 decisions for Titan Implants (Flemington, NJ) from 2001 to 2005: 4 510(k) clearances. Most are in product codes DZE (Implant, Endosseous, Root-Form) and NHA (Abutment, Implant, Dental, Endosseous). Its devices cite 17 predicates, 1 of them its own earlier devices. No recall is linked to its devices.

FDA’s records also spell it “Titan Implants, Inc.”.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, dental panel, where it files most

How often FDA has decided Titan Implants’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Titan Implants since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Titan Implants’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

Other applicant names beginning “Titan”

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

Titan Spine, LLC 19 Titan Tables 4 Titan Medical, Inc. 3 Titan Mfg., Inc. 3 Titan Condoms, LLC 2 Titan Manufacturing, Inc. 1 Titan Technology Intl., Inc. 1

Titan Implants

Which product codes does it file in?

Whose devices does it build on?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Titan”