FDA applicant

Titan Medical, Inc.

Arden Hills, MN3 decisions1987–19880 recalls

FDA records 3 decisions for Titan Medical, Inc. (Arden Hills, MN) from 1987 to 1988: 3 510(k) clearances. Most are in product codes LJT (Port & Catheter, Implanted, Subcutaneous…) and DYB (Introducer, Catheter). 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 hospital panel, where it files most

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

FDA decisions per year

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

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Titan Medical, 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 Mfg., Inc. 3 Titan Condoms, LLC 2 Titan Manufacturing, Inc. 1 Titan Technology Intl., Inc. 1

Titan Medical, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Titan”