Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3010626738

FEI Number

3010626738

Entity Name

BIOMOBIE (SHANGHAI) REGENERATIVE MEDICINE CO., LTD.

City/State/Country

Shanghai, CN

Establishment Address

1388 Kaixuan Rd,, IM Shanghai,T1, FL,Unit704,Shanghai, Shanghai 201199, CN

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Biomobie (Shanghai) Regenerative Medicine Co., Ltd. (Owner Number: 10045762)

Owner / Operator Contact Address

Suite 310,320,327, No.1 Building, 18 Shenwang Rd., Minhang District, Shanghai, CN-SH 201108, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Bioboosti, BBT-I, BBT-II

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
ISA	Massager, Therapeutic, Electric	Physical Medicine	Class 1	890.5660	2013-12-24

Official Correspondent

Ally Miao

US Agent Details

Rebecca Toman Email: cs@ltlqa.com Phone: (281) 6008227

Related Public Records

Same Entity

Biomobie (Shanghai) Regenerative Medicine Co., Ltd.

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

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010626738. Last updated year: 2026. Please use registration number 3010626738 when referencing this establishment in official correspondence.