510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K141452Substantially Equivalent

Leforte Neuro System Bone Plate and Screw

Jeil Medical Corporation, Fullerton CA / Special, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K141452 is the FDA 510(k) clearance record for LEFORTE NEURO SYSTEM BONE PLATE AND SCREW, a class II device, cleared for Jeil Medical Corporation on under FDA product code GWO (Plate, Cranioplasty, Preformed, Alterable). FDA records list 53 510(k) clearances for Jeil Medical Corporation, from to . As of , FDA records show no recalls naming K141452.

Clearance record

Decision date
Received
(30 days to decision)
Product code
GWO Plate, Cranioplasty, Preformed, Alterable
Regulation
21 CFR 882.5320
Device class
Class II
Review panel
Neurology
Applicant
Jeil Medical Corporation 2651 E. Chapman Ave., Suite 110, Fullerton CA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code GWO

Trailing 12 months
2 clearances under product code GWO in the twelve months to October 2026, July 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code GWO, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20261
August 20260
September 20261
October 20260