510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K240002Substantially Equivalent

G-Vitri™ Vitrification Straw

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

K240002 is the FDA 510(k) clearance record for G-Vitri™ Vitrification Straw, a class II device, cleared for Gimbo Medical Technology Shenzhen Co., Ltd. on under FDA product code MQK (Labware, Assisted Reproduction). FDA records list 7 510(k) clearances for Gimbo Medical Technology Shenzhen Co., Ltd., from to . As of , FDA records show no recalls naming K240002.

Clearance record

Decision date
Received
(164 days to decision)
Product code
MQK Labware, Assisted Reproduction
Regulation
21 CFR 884.6160
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 MQK

Trailing 12 months

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

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