510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K232942Substantially Equivalent

G-Vitri™ Vitrification Freeze Media; G-Vitri™ Vitrification Thawing Media

Gimbo Medical Technology Shenzhen Co., Ltd., Shenzhen, CN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K232942 is the FDA 510(k) clearance record for G-Vitri™ Vitrification Freeze Media; G-Vitri™ Vitrification Thawing Media, a class II device, cleared for Gimbo Medical Technology Shenzhen Co., Ltd. on under FDA product code MQL (Media, Reproductive). FDA records list 7 510(k) clearances for Gimbo Medical Technology Shenzhen Co., Ltd., from to . As of , FDA records show no recalls naming K232942.

Clearance record

Decision date
Received
(132 days to decision)
Product code
MQL Media, Reproductive
Regulation
21 CFR 884.6180
Device class
Class II
Review panel
Obstetrics/Gynecology
Applicant
Gimbo Medical Technology Shenzhen Co., Ltd. 601, Bldg. C5, # 459 Qiaokai Rd., Fenghuang St.,, Shenzhen, CN
510(k) summary
Statement
Third party review
No

Clearances, product code MQL

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