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menovex Medical Technology (Shenzhen) Co., Ltd

Shenzhen Guangdong, CN

menovex Medical Technology (Shenzhen) Co., Ltd appears in FDA device records in Shenzhen Guangdong, CN. FDA records list one 510(k) clearance, no PMA records and one registered establishment. As of , FDA records show no recalls for this company, and at least one establishment registration is current.

FDA records held for this company

510(k) clearances
1
PMA records
0
Recall records
0
Registered establishments
1

510(k) clearance history

FDA records hold 1 510(k) clearance for menovex Medical Technology (Shenzhen) Co., Ltd in 2025.

Clearances by year, as a table
510(k) clearance decisions for menovex Medical Technology (Shenzhen) Co., Ltd, by decision year
YearClearances
20251
510(k) clearances on record, most recent first
K numberDeviceProduct codeDecisionDecision date
K251303Tamburo Thulium Fiber Laser SystemGEXSubstantially Equivalent

Registered establishments

FDA registered establishments for menovex Medical Technology (Shenzhen) Co., Ltd, with the product codes listed at each
RegistrationFEIEstablishmentAddressRegistration expiresProduct codes listed
30422624963042262496menovex Medical Technology (Shenzhen) Co., Ltd401, 501, Building 13, Biomedicine Innovation Industrial Park, No. 14, Jinhui Road, Shenzhen Guangdong 518118 CN2026

Registration numbers link to the FDA registration and listing record for that establishment.

FDA product codes

Recall records

No recall records for this company in the ingested FDA data.

Verification record

There is no verification record for this company. Most companies on this site have none: a record exists only where a company asked to be verified and MDM ran the checks, so the absence of one says nothing about the company.

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What MDM checks, and what it does not

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Data as of , FDA export datePage updated Source: openFDA, public domain