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
K820567Substantially Equivalent

Trep Card Eiken

Syn-Kit, Inc., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K820567 is the FDA 510(k) clearance record for TREP CARD EIKEN, a class II device, cleared for Syn-Kit, Inc. on under FDA product code GMQ (Antigens, Nontreponemal, All). FDA records list 34 510(k) clearances for Syn-Kit, Inc., from to . As of , FDA records show no recalls naming K820567.

Clearance record

Decision date
Received
(43 days to decision)
Product code
GMQ Antigens, Nontreponemal, All
Regulation
21 CFR 866.3820
Device class
Class II
Review panel
Microbiology
Applicant
Syn-Kit, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code GMQ

Trailing 12 months

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

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