FDA applicant

Promedica, Inc.

Oldsmar, FL2 decisions2004–20040 recalls

FDA records 2 decisions for Promedica, Inc. (Oldsmar, FL) in 2004: 2 510(k) clearances. All are in product code KCT (Sterilization Wrap Containers, Trays…). 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 Promedica, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Promedica, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Promedica, 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 “Promedica”

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

Promedica Products, Inc. 6 Promedica Sdn. Bhd. 1

Promedica, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Promedica”