510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K020560Substantially Equivalent

Workbench by <Genx>

<Genx> Intl., Inc., Gilford CT / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K020560 is the FDA 510(k) clearance record for WORKBENCH BY <GENX>, a class II device, cleared for Genx Intl., Inc. on under FDA product code MQG (Accessory, Assisted Reproduction). FDA records list 32 510(k) clearances for Genx Intl., Inc., from to . As of , FDA records show no recalls naming K020560.

Clearance record

Decision date
Received
(119 days to decision)
Product code
MQG Accessory, Assisted Reproduction
Regulation
21 CFR 884.6120
Device class
Class II
Review panel
Obstetrics/Gynecology
Applicant
Genx Intl., Inc. 393 Soundview Rd., Gilford CT
510(k) summary
Statement
Third party review
No

Clearances, product code MQG

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