Medical Device Manufacturer · US , Houston , TX

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

3 submissions · 3 cleared · Since 1988

3

Total

3

Cleared

0

Denied

FDA 510(k) Regulatory Record - Technitex, Inc. Ophthalmic ✕

3 devices

1-3 of 3

Cleared Sep 11, 1989

VKG 2000 VIDEO KERATOMETER

Ophthalmic · 101d

Cleared Nov 08, 1988

VKG 1000, VIDEO KERATOMETER

Ophthalmic · 84d

Cleared Aug 04, 1988

QRK 100, QUALITATIVE RING KERATOSCOPE

Ophthalmic · 23d