Medical Device Manufacturer · US , Salt Lake City , UT

Sorex Medical - FDA 510(k) Cleared Devices

9 submissions · 6 cleared · Since 1989

Total

Cleared

Denied

Sorex Medical has 6 FDA 510(k) cleared medical devices. Based in Salt Lake City, US.

Historical record: 6 cleared submissions from 1989 to 1994. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Sorex Medical Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Sorex Medical

9 devices

1-9 of 9

Cleared Mar 25, 1994

FOGLESS

K923843 · OCT

Gastroenterology & Urology · 602d

Cleared Sep 06, 1991

PLUME MASTER

K913036 · FYD

General Hospital · 59d

Cleared Jul 05, 1991

PICC-FIX

K911070 · KMK

General Hospital · 116d

Cleared Jun 28, 1991

SOREX SAFE-AIR

K911150 · GEX

General & Plastic Surgery · 105d

Cleared Apr 05, 1991

PICC INSERTION KIT/P.I.C. & PICC EXCHANG KIT/P.E.K

K910315 · LJS

General Hospital · 71d

Cleared Mar 12, 1991

EDLICH WOUND MANAGEMENT TRAY

K905572 · MCY

General & Plastic Surgery · 90d

Cleared Dec 06, 1990

TRACH-EZE

K903740 · BSY

Anesthesiology · 112d

Cleared Nov 20, 1990

MEDICAL PROCEDURE TRAY

K902410 · LDQ

General & Plastic Surgery · 173d

Cleared Feb 06, 1989

GRAFT GUARD

K885136 · LZM

General & Plastic Surgery · 53d

Sorex Medical - FDA 510(k) Cleared Devices

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