Karlin Technology, Inc.
Karlin Technology, Inc. holds FDA 510(k) medical device clearances, first cleared 1988, most recent 1990.
Top product codes for Karlin Technology, Inc.
Recent clearances by Karlin Technology, Inc.
- K903969 — SUCTION RETRACTOR(TOWER ATTACH.)FOR CRANK FRAM RET
- K893201 — BONE PLATE
- K893203 — BONE SCREW
- K882525 — SPINAL MICROKNIFE
- K882519 — X-RAY MARKER
- K882073 — SPINAL NEEDLE
- K882520 — SHOULDER BOLSTER, KNEE, ANKLE & LEG SUPPORT PADS
- K882524 — UNIVERSALLY ADJUSTABLE ARMBOARD
- K882069 — SPINAL DISTRACTORS, SPANNERS
- K882072 — ORTHOPAEDIC AND SPINAL RING CURRETTES
- K882077 — MICRODISCECTOMY CURRETTES
- K882074 — SUCTION RETRACTORS
- K882075 — SELF-RETAINING SOFT TISSUE RETRACTOR
- K882078 — SPINAL SURGERY FRAME
- K882071 — CRANK FRAME RETRACTOR
- K882068 — COBB SPINAL ELEVATORS
- K882070 — LUMBAR IMPACTION SET AND BONE GRAFT IMPACTORS
Data sourced from openFDA. This site is unofficial and independent of the FDA.