510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K896589Substantially Equivalent

Manual Surgical Instruments for Titamed Antwerp

Optik, Criftib MD / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K896589 is the FDA 510(k) clearance record for MANUAL SURGICAL INSTRUMENTS FOR TITAMED ANTWERP, a class I device, cleared for Optik on under FDA product code LRZ (Screwdriver, Surgical). FDA records list 4 510(k) clearances for Optik, from to . As of , FDA records show no recalls naming K896589.

Clearance record

Decision date
Received
(36 days to decision)
Product code
LRZ Screwdriver, Surgical
Regulation
21 CFR 878.4800
Device class
Class I
Review panel
General, Plastic Surgery
Applicant
Optik 2131espey Ct., Criftib MD
Third party review
No

Clearances, product code LRZ

Trailing 12 months

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

FDA records show no clearances under product code LRZ in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code LRZ, 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