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
K210099Substantially Equivalent

Meticuly Patient-Specific Titanium Mesh Implant

Meticuly Co., Ltd., Muang Nonthaburi, TH / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K210099 is the FDA 510(k) clearance record for Meticuly Patient-Specific Titanium Mesh Implant, a class II device, cleared for Meticuly Co., Ltd. on under FDA product code GXN (Plate, Cranioplasty, Preformed, Non-Alterable). FDA records list 4 510(k) clearances for Meticuly Co., Ltd., from to . As of , FDA records show no recalls naming K210099.

Clearance record

Decision date
Received
(341 days to decision)
Product code
GXN Plate, Cranioplasty, Preformed, Non-Alterable
Regulation
21 CFR 882.5330
Device class
Class II
Review panel
Neurology
Applicant
Meticuly Co., Ltd. 32/77, Soi Samakkee 58/20, Samakkee Rd., Tasai, Muang Nonthaburi, TH
510(k) summary
Summary PDF
Third party review
No

Clearances, product code GXN

Trailing 12 months
6 clearances under product code GXN in the twelve months to October 2026, November 2025 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code GXN, trailing twelve months
MonthClearances
November 20252
December 20250
January 20261
February 20260
March 20260
April 20261
May 20260
June 20262
July 20260
August 20260
September 20260
October 20260