Medical Device Manufacturer · US , San Antonio , TX

Teftec Corp. - FDA 510(k) Cleared Devices

8 submissions · 8 cleared · Since 1996

Recent clearances: ALPHATRAC, MODEL A 205, OMEGATRAC, MODEL Z105, OMEGA TRAC, MODEL Z100

View 8 510(k) Devices ↓

Total

Cleared

Denied

Teftec Corp. has 8 FDA 510(k) cleared medical devices. Based in San Antonio, US.

Historical record: 8 cleared submissions from 1996 to 2002. Primary specialty: Physical Medicine.

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

Teftec Corp. is one of 21726 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Teftec Corp.

8 devices

1-8 of 8

Cleared Nov 21, 2002

ALPHATRAC, MODEL A 205

K022652 · ITI

Physical Medicine · 104d

Cleared Feb 08, 2002

OMEGATRAC, MODEL Z105

K013307 · ITI

Physical Medicine · 127d

Cleared Nov 18, 1999

OMEGA TRAC, MODEL Z100

K993160 · ITI

Physical Medicine · 58d

Cleared Oct 25, 1999

FIRST CLASS POWER RECLINE SEATING SYSTEM, MODEL S500

K992627 · ITI

Physical Medicine · 81d

Cleared Oct 25, 1999

FIRSTCLASS POWER TILT AND RECLINE SEAT SYSTEM, MODEL S400

K992628 · ITI

Physical Medicine · 81d

Cleared Nov 27, 1998

FIRSTCLASS POWER TILT SEAT SYSTEM, MODEL S300

K983066 · ITI

Physical Medicine · 86d

Cleared Nov 06, 1998

ALPHATRAC, MODEL A200

K982815 · ITI

Physical Medicine · 87d

Cleared Jul 01, 1996

OMEGATRAC BY TEFTEC

K955240 · ITI

Physical Medicine · 230d

Teftec Corp. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Teftec Corp.

Filters