510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K882069Substantially Equivalent

Spinal Distractors, Spanners

Karlin Technology, Inc., Marina Del Rey CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K882069 is the FDA 510(k) clearance record for SPINAL DISTRACTORS, SPANNERS, a class I device, cleared for Karlin Technology, Inc. on under FDA product code LXH (Orthopedic Manual Surgical Instrument). FDA records list 17 510(k) clearances for Karlin Technology, Inc., from to . As of , FDA records show no recalls naming K882069.

Clearance record

Decision date
Received
(31 days to decision)
Product code
LXH Orthopedic Manual Surgical Instrument
Regulation
21 CFR 888.4540
Device class
Class I
Review panel
Orthopedic
Applicant
Karlin Technology, Inc. 330 Washington St., Marina Del Rey CA
Third party review
No

Clearances, product code LXH

Trailing 12 months

FDA records hold no clearances under product code LXH in the trailing twelve months.

FDA records show no clearances under product code LXH in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code LXH, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260