Data / Medical devices / Denmark / Ferrosan Medical Devices A/S

Ferrosan Medical Devices A/S: FDA-registered device maker in Soeborg Hovedstaden, Denmark, 1 PMA approval

Ferrosan Medical Devices A/S is registered with the FDA (registration 3008478369) in Soeborg Hovedstaden, Denmark. It lists 1 device type. The FDA files 1 PMA approval under its listings, the newest dated September 30, 1999. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number

3008478369

Address

Sydmarken 5, Soeborg Hovedstaden, Denmark, 2860

Owner or operator

Ferrosan Medical Devices A/S (10032756)

Roles

Manufacturer

First device listed

June 16, 2010

Registered through

2026

Brand names listed

SURGIFLO Hemostatic Matrix, SURGIFOAM Absorbable Gelatin Powder, SURGIFOAM Absorbable Gelatin Sponge

Devices it lists

PMA approvals

Premarket approvals this establishment lists, with the supplements the FDA has decided since.

Compare with other makers

• All makers of Agent, Absorbable Hemostatic, Collagen Based

Updated September 18, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.