Medical Device Manufacturer · US , Mchenry , IL

Spenco Medical Corp. - FDA 510(k) Cleared Devices

10 submissions · 9 cleared · Since 1979

Total

Cleared

Denied

Spenco Medical Corp. has 9 FDA 510(k) cleared general & plastic surgery devices. Based in Mchenry, US.

Historical record: 9 cleared submissions from 1979 to 1998.

Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.

Spenco Medical Corp. 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 - Spenco Medical Corp.

10 devices

1-10 of 10

Cleared Jun 25, 1998

SPENCO SILICONE GEL SHEET

K981902 · MDA

General & Plastic Surgery · 24d

Cleared Dec 11, 1992

2ND SKIN STERILE ADHESIVE STRIP

K922228 · KGX

General & Plastic Surgery · 213d

Cleared Sep 06, 1991

2ND SKIN MOIST BURN PADS WITH ALOE

K911550 · MGQ

General & Plastic Surgery · 151d

Cleared Jun 03, 1991

SPENCIO SKIN GUARD KIT

K910927 · KMF

General & Plastic Surgery · 90d

Cleared Dec 13, 1989

SPENCO BREAST FORMS

K896533 · KCZ

General & Plastic Surgery · 29d

Cleared Aug 23, 1989

2ND SKIN NON-STICK MOIST BURN PADS

K894898 · FRO

General & Plastic Surgery · 22d

Cleared May 13, 1982

SPENCO CRYOPRESS

K820906 · IMD

Physical Medicine · 42d

Cleared May 20, 1981

SPENCO DERMAL PADS

K811184 · FMP

General Hospital · 21d

Cleared Nov 20, 1979

HYDROGEL-PREP

K791726 · NAB

General & Plastic Surgery · 77d

Cleared Sep 04, 1979

GELSKIN

K791162 · ILO

Physical Medicine · 71d

Spenco Medical Corp. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Spenco Medical Corp.

Filters