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
K042426Substantially Equivalent

Tmd 0.5Ml Safety Syringe (Fa18 Series 0.5Ml/fa58 Series U-100 Insulin/fa78 Series Tuberculin)

Taiject Medical Device Co., Ltd., Newport Beach CA / Special, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K042426 is the FDA 510(k) clearance record for TMD 0.5ML SAFETY SYRINGE (FA18 SERIES 0.5ML/FA58 SERIES U-100 INSULIN/FA78 SERIES TUBERCULIN), a class II device, cleared for Taiject Medical Device Co., Ltd. on under FDA product code MEG (Syringe, Antistick). FDA records list 4 510(k) clearances for Taiject Medical Device Co., Ltd., from to . As of , FDA records show no recalls naming K042426.

Clearance record

Decision date
Received
(14 days to decision)
Product code
MEG Syringe, Antistick
Regulation
21 CFR 880.5860
Device class
Class II
Review panel
General Hospital
Applicant
Taiject Medical Device Co., Ltd. P.O. Box 8853, Newport Beach CA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code MEG

Trailing 12 months
2 clearances under product code MEG in the twelve months to October 2026, December 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code MEG, trailing twelve months
MonthClearances
November 20250
December 20251
January 20260
February 20261
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260