Medical Device Manufacturer · US , Arvada , CO

Dermaphylyx, Inc. - FDA 510(k) Cleared Devices

9 submissions · 7 cleared · Since 1999

Total

Cleared

Denied

Dermaphylyx, Inc. has 7 FDA 510(k) cleared medical devices. Based in Arvada, US.

Historical record: 7 cleared submissions from 1999 to 1999. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Dermaphylyx, Inc. Filter by specialty or product code using the sidebar.

Dermaphylyx, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Dermaphylyx, Inc.

9 devices

1-9 of 9

Cleared Sep 14, 1999

DERMAPHYLYX SKIN PROTECTORS, PROTECT IT SKIN PROTECTORS

K992302 · MGP

General & Plastic Surgery · 68d

Cleared Aug 12, 1999

DERMAPHYLYX HYDROPHILIC FOAM WOUND DRESSING

K991920 · KMF

General & Plastic Surgery · 66d

Cleared Jul 30, 1999

DERMAPHYLYX FOAM ISLAND DRESSING

K991933 · KMF

General & Plastic Surgery · 52d

Cleared Jul 20, 1999

DERMAPHYLYX CALCIUM ALGINATE WOUND DRESSING

K991608 · KMF

General & Plastic Surgery · 71d

Cleared Jul 20, 1999

DERMAPHYLYX SUPER ABSORBENT FIBER DRESSING

K991609 · KMF

General & Plastic Surgery · 71d

Cleared Jun 28, 1999

DERMAPHYLYX CALCIUM ALGINATE WOUND DRESSING

K991061 · NAE

General & Plastic Surgery · 90d

Cleared May 27, 1999

DERMAPHYLYX FILM WOUND DRESSING AND HEALIAN FILM WOUND DRESSING

K990875 · MGP

General & Plastic Surgery · 72d

Cleared May 27, 1999

DERMAPHYLYX HYDROCOLLOID WOUND DRESSING, HEALIAN HYDROCOLLOID WOUND DRESSING

K990891 · FRO

General & Plastic Surgery · 71d

Cleared Mar 25, 1999

DERMAFLEX WOUND DRESSING, DERMAFLEX FOAM WOUND DRESSING, HEALIAFLEX WOUND...

K990438 · MGP

General & Plastic Surgery · 42d

Dermaphylyx, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Dermaphylyx, Inc.

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