510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K923419Substantially Equivalent

Tismesh System

Ti-Mesh, Inc., Las Vegas NV / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K923419 is the FDA 510(k) clearance record for TISMESH SYSTEM, a class II device, cleared for Ti-Mesh, Inc. on under FDA product code JEY (Plate, Bone). FDA records list 3 510(k) clearances for Ti-Mesh, Inc., from to . As of , FDA records show no recalls naming K923419.

Clearance record

Decision date
Received
(269 days to decision)
Product code
JEY Plate, Bone
Regulation
21 CFR 872.4760
Device class
Class II
Review panel
Dental
Applicant
Ti-Mesh, Inc. 76 Spectrum Rd., Las Vegas NV
510(k) summary
Statement
Third party review
No

Clearances, product code JEY

Trailing 12 months
5 clearances under product code JEY in the twelve months to October 2026, November 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code JEY, trailing twelve months
MonthClearances
November 20251
December 20251
January 20260
February 20260
March 20260
April 20261
May 20260
June 20260
July 20261
August 20261
September 20260
October 20260