510(k) Report

FDA applicant

Medic Group of Scandinavia, Inc.

Washington, DC1 decision1985–19850 recalls

FDA records 1 decision for Medic Group of Scandinavia, Inc. (Washington, DC) in 1985: 1 510(k) clearance. No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

How often FDA has decided Medic Group of Scandinavia, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Medic Group of Scandinavia, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Medic Group of Scandinavia, 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 “Medic”

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