FDA applicant

Ttl Medical

Knoxville, TN2 decisions1995–19950 recalls

FDA records 2 decisions for Ttl Medical (Knoxville, TN) in 1995: 2 510(k) clearances. Most are in product codes MGP (Dressing, Wound And Burn, Occlusive) and FPX (Strip, Adhesive, Closure, Skin). 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 Ttl Medical’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Ttl Medical since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Ttl Medical’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

Ttl Medical

Which product codes does it file in?

What has FDA decided for it lately?