Medical Device Manufacturer · US , Marina Del Rey , CA

Karlin Technology, Inc. - FDA 510(k) Cleared Devices

17 submissions · 17 cleared · Since 1988

Total

Cleared

Denied

Karlin Technology, Inc. has 17 FDA 510(k) cleared medical devices. Based in Marina Del Rey, US.

Historical record: 17 cleared submissions from 1988 to 1990. Primary specialty: Orthopedic.

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

FDA 510(k) Regulatory Record - Karlin Technology, Inc.

17 devices

1-12 of 17

Cleared Sep 05, 1990

SUCTION RETRACTOR(TOWER ATTACH.)FOR CRANK FRAM RET

K903969 · GAD

General & Plastic Surgery · 8d

General & Plastic Surgery · 62d

Cleared Jul 18, 1988

SHOULDER BOLSTER, KNEE, ANKLE & LEG SUPPORT PADS

K882520 · LWG

General & Plastic Surgery · 31d

Cleared Jul 08, 1988

UNIVERSALLY ADJUSTABLE ARMBOARD

K882524 · BTX

General & Plastic Surgery · 21d

Cleared Jun 17, 1988

SPINAL DISTRACTORS, SPANNERS

K882069 · LXH

Orthopedic · 31d

Cleared Jun 17, 1988

ORTHOPAEDIC AND SPINAL RING CURRETTES

K882072 · JXH

Neurology · 31d

Cleared Jun 17, 1988

MICRODISCECTOMY CURRETTES

General & Plastic Surgery · 30d

Karlin Technology, Inc. - FDA 510(k) Cleared Devices

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