FDA applicant

Titan Technology Intl., Inc.

St. Louis, MI1 decision1991–19910 recalls

FDA records 1 decision for Titan Technology Intl., Inc. (St. Louis, MI) in 1991: 1 510(k) clearance. All are in product code JFB (Table, Physical Therapy, Multi Function). 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, physical medicine panel, where it files most

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

FDA decisions per year

No FDA decision for Titan Technology Intl., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Titan 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 “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 Mfg., Inc. 3 Titan Condoms, LLC 2 Titan Manufacturing, Inc. 1

Titan Technology Intl., Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Titan”