Ferrosan Meidcal Devices A S

FDA Filings

This page includes the latest FDA filings for Ferrosan Meidcal Devices A S. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Filings

Device Company	Device	Date
PMA P990004S053 Ferrosan Meidcal Devices A/S	SURGIFLO® Hemostatic Matrix Kit with Thrombin	2022-01-21
PMA P990004S052 Ferrosan Meidcal Devices A/S	SURGIFOAM® Absorbable Gelatin Sponge, SURGIFLO® Hemostatic Matrix, SURGIFOAM® Absorbable Gelatin Powder, SURGIFOAM® Abso	2022-01-19
PMA P990004S051 Ferrosan Meidcal Devices A/S	SURGIFOAM® Absorbable Gelatin Sponge, U.S.P., Dental Sponge, SURGIFOAM® Absorbable Gelatin Sponge, U.S.P., Hemorrhoidect	2021-12-21
PMA P990004S050 Ferrosan Meidcal Devices A/S	SURGIFOAM® Absorbable Gelatin Sponge, U.S.P.	2021-10-28
PMA P990004S049 Ferrosan Meidcal Devices A/S	SURGIFOAM® Absorbable Gelatin Sponge, U.S.P.	2021-08-25
PMA P990004S048 Ferrosan Meidcal Devices A/S	SURGIFOAM Absorbable Gelation Sponge, U.S.P.	2021-06-02
PMA P990004S047 Ferrosan Meidcal Devices A/S	SURGIFOAM® Absorbable Gelatin Sponge, U.S.P., Hemorrhoidectomy Sponge/Oral Sponge and SURGIFOAM® Absorbable Gelatin Powd	2021-04-30
PMA P990004S043 Ferrosan Meidcal Devices A/S	SURGIFOAM Absorbable Gelatin Sponge, U.S.P.	2020-09-25
PMA P990004S042 Ferrosan Meidcal Devices A/S	SURGIFOAM Absorbable Gelatin Sponge U.S.P.	2020-08-27
PMA P990004S041 Ferrosan Meidcal Devices A/S	SURGIFOAM Absorbable Gelatin Sponge, U.S.P.	2020-07-24
PMA P990004S040 Ferrosan Meidcal Devices A/S	SURGIFOAM Absorbable Gelatin Sponge, U.S.P.	2020-07-08
PMA P990004S038 Ferrosan Meidcal Devices A/S	SURGIFOAM Absorbable Gelatin Sponge, U.S.P.	2020-04-14
PMA P990004S037 Ferrosan Meidcal Devices A/S	SURGIFOAM Absorbable Gelatin Sponge, U.S.P.	2020-03-19

Similar & Related FDA Registered Companies

• Ferrosan Meidcal Devices A/Ssydmarken 5soeborg 08876 PMA NumberP990004 Supplement NumberS056 Date Received07/01/2022 Decision Date01/31/2023 Product Code LMF  Advisory Committee General & Plastic Surgery Supplement Type135 Review Track For 30-day Notice Supplement Reason Process Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No
• Ferrosan Meidcal Devices A/Ssydmarken 5soeborg 08876 PMA NumberP990004 Supplement NumberS055 Date Received06/27/2022 Decision Date12/21/2022 Product Code LMF  Advisory Committee General & Plastic Surgery Supplement Type135 Review Track For 30-day Notice Supplement Reason Process Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No
• Ferrosan Meidcal Devices A/Ssydmarken 5soeborg 08876 PMA NumberP990004 Supplement NumberS054 Date Received03/07/2022 Decision Date04/06/2022 Product Code LMF  Advisory Committee General & Plastic Surgery Supplement Type30-day Notice Supplement Reason Process Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No