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Shenzhen Trious Medical Technology Co., Ltd

Shenzhen Guangdong, CN

SHENZHEN TRIOUS MEDICAL TECHNOLOGY CO., LTD appears in FDA device records in Shenzhen Guangdong, CN. FDA records list 3 510(k) clearances between and , 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
3
PMA records
0
Recall records
0
Registered establishments
1

510(k) clearance history

FDA records hold 3 510(k) clearances for Shenzhen Trious Medical Technology Co., Ltd in 2025.

Clearances by year, as a table
510(k) clearance decisions for Shenzhen Trious Medical Technology Co., Ltd, by decision year
YearClearances
20253
510(k) clearances on record, most recent first
K numberDeviceProduct codeDecisionDecision date
K250448Disposable Percutaneous Nephrostomy Dilatation KitLJESubstantially Equivalent
K243830Disposable ureteral stentFADSubstantially Equivalent
K243710Disposable ureteral access sheathFEDSubstantially Equivalent

Registered establishments

FDA registered establishments for Shenzhen Trious Medical Technology Co., Ltd, with the product codes listed at each
RegistrationFEIEstablishmentAddressRegistration expiresProduct codes listed
30338482083033848208SHENZHEN TRIOUS MEDICAL TECHNOLOGY CO., LTDRm B102 Bldg B4 Rm 401 402 Bldg D3 YingZhan S T Estate Longtian Tongfuyu Rd 8, 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

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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