Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3030019986

FEI Number

3030019986

Entity Name

QuantMed LifeTech (Shenzhen) Co., Ltd.

City/State/Country

ShenzhenCity Guangdong, CN

Establishment Address

Room 202, Huigu, Meisheng Chuanggu Phase II, Longchang Road, Bao, Room 1101, Shenzhen Bay Venture Capital Building, Haitian 2nd Road, Nanshan District, Shenzhen City, Guangdong, ShenzhenCity Guangdong 518101, CN

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

QuantMed LifeTech (Shenzhen) Co., Ltd. (Owner Number: 10088960)

Owner / Operator Contact Address

Room 202, Huigu, Meisheng Chuanggu Phase II, Longchang Road, Baoan District, Shenzhen City, Guangdong Province, Shenzhen, CN-GD 518133, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Adaptive spinal protection Flex Bed Base BED, PEDIATRIC OPEN HOSPITAL Mattress, air flotation, alternating pressure Orthosis, cervical

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
LLI	Bed, Therapeutic, Ac-Powered, Adjustable Home-Use	General Hospital	Class 2	880.5100	2024-12-31
FMS	Bed, Pediatric Open Hospital	General Hospital	Class 2	880.5140	2023-10-25
FNM	Mattress, Air Flotation, Alternating Pressure	General Hospital	Class 2	880.5550	2023-10-25
IQK	Orthosis, Cervical	Physical Medicine	Class 1	890.3490	2023-10-25

Official Correspondent

Lina Wang

US Agent Details

Leeyeo Kee Business: Regrek LLC Email: regrek.cs@hotmail.com Phone: (302) 6089028

Related Public Records

Same Entity

QuantMed LifeTech (Shenzhen) Co., Ltd.

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0006-2025	Ossur H F Grjothals 5 Reykjavik Iceland	1	Miami J Select Collar, Catalog: MJS-101; Miami J Select Collar Set, Catalog: MJSR-101

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3030019986. Last updated year: 2026. Please use registration number 3030019986 when referencing this establishment in official correspondence.