FDA applicant

Titan Mfg., Inc.

Phoenixville, PA3 decisions1998–19980 recalls

FDA records 3 decisions for Titan Mfg., Inc. (Phoenixville, PA) in 1998: 3 510(k) clearances. All are in product code HTD (Forceps). 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, general and plastic surgery panel, where it files most

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

FDA decisions per year

No FDA decision for Titan Mfg., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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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 Implants 4 Titan Medical, Inc. 3 Titan Condoms, LLC 2 Titan Manufacturing, Inc. 1 Titan Technology Intl., Inc. 1

Titan Mfg., 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?

Other applicant names beginning “Titan”