Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3009557417

FEI Number

3009557417

Entity Name

WENZHOU LINGFENG ELECTRONIC TECHNOLOGY CO., LTD

City/State/Country

Ruian Zhejiang, CN

Establishment Address

NO.6 PUXI INDUSTRY ZONE, TONGPU, Ruian Zhejiang 325216, CN

Establishment Type(s)

Export Device to the United States But Perform No Other Operation on Device,Manufacture Medical Device

Owner / Operator

WENZHOU LINGFENG ELECTRONIC TECHNOLOGY CO., LTD (Owner Number: 10040198)

Owner / Operator Contact Address

NO.6 PUXI INDUSTRY ZONE, TONGPU, RUIAN, CN-ZJ 325216, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Air Compression Massager models UM01.UM02.UM03.UM04.UM05.UM06 Air Compression Massager models BG01.BG02.BG03.BG04.BG05.BG06 Air Compression Massager models LF001.LF002.LF003.LF004.LF005.LF006 Air Compression Massager models LF-FT001.LF-FT002.LF-FT003.LF-FT004.LF-FT005.LF-FT006 Air Compression Massager models AI01.AI02.AI03.AI04.AI05.AI06 Air Compression Massager models LF-FT004;LF-FT005;LF-FT006; LF001;LF002;LF003;LF004;LF005;LF006;UM-01;UM-02;UM-03;UM-04 Air Compression Massager models AI-01;AI-02;AI-03;AI-04;AI-05;AI-06; LF-FT001;LF-FT001-1;LF-FT002;LF-FT002-1;LF-FT003; Air Compression Massager models UM-05;UM-06 Massage Pillow Massage Chair Massage Hammer Foot Massager Massager Brush Massage Cushion Office & Leisure Chair Massage Mattress Eye Massager Massage Belt UM-04-1, UM-05-1, UM-06-1, UM-07, UM-08, UM-09, UM-10, UM-11, UM-12, UM-13, UM-14, UM-15, UM-16, AI-01, AI-02, AI-03, Air Compression Leg Massager: LF-FT001, LF-FT002-1, LF-FT003, LF-FT003-1, LF-FT004-1, LF-FT005-1, LF-FT006-1, LF-FT007 AI-04, AI-05, AI-06, AI01, AI02, AI03, AI-07, AI-08, AI-09, AI-10, AI-11, AI-12, AI-13, AI-14. LF-FT008, LF-FT009, LF-FT010, LF-FT011, LF-FT012, LF-FT013, LF-FT014, LF-FT015, LF-FT016, UM-01, UM-02, UM-03, UM-03-1, Air Compression Massager models LF-FT001.LF-FT002.LF-FT003.LF-FT004.LF-FT005.LF-FT006 Air Compression Massager models BG01.BG02.BG03.BG04.BG05.BG06 Air Compression Massager models UM-05;UM-06 Air Compression Massager models LF-FT004;LF-FT005;LF-FT006; LF001;LF002;LF003;LF004;LF005;LF006;UM-01;UM-02;UM-03;UM-04 Air Compression Massager models: LF-FT003 Air Compression Massager models AI01.AI02.AI03.AI04.AI05.AI06 Air Compression Massager models UM01.UM02.UM03.UM04.UM05.UM06 Heating Pad Air Compression Massager models LF001.LF002.LF003.LF004.LF005.LF006 Air Compression Massager models AI-01;AI-02;AI-03;AI-04;AI-05;AI-06; LF-FT001;LF-FT001-1;LF-FT002;LF-FT002-1;LF-FT003;

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
IRP	Massager, Powered Inflatable Tube	Physical Medicine	Class 2	890.5650	2021-11-18
ISA	Massager, Therapeutic, Electric	Physical Medicine	Class 1	890.5660	2012-03-18
IRO	Vibrator, Therapeutic	Physical Medicine	Class 1	890.5975	2012-03-18
IRP	Massager, Powered Inflatable Tube	Physical Medicine	Class 2	890.5650	2026-05-11
IRT	Pad, Heating, Powered	Physical Medicine	Class 2	890.5740	2026-05-11
IRT	Pad, Heating, Powered	Physical Medicine	Class 2	890.5740	2025-03-10

Official Correspondent

No official correspondent registered.

US Agent Details

Charles Mack Business: IRC USA Email: ircfda@gmail.com Phone: (931) 6254938

Related Public Records

Same Entity

WENZHOU LINGFENG ELECTRONIC TECHNOLOGY CO., LTD

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

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K242140	Jiale Health Technology Shenzhen Co., Ltd.	Air Compression Leg Massager (K-705)	2025-03-17
K821133	Durham Electric Co.	ELECTRICAL VIBRATING DEVICE	1982-07-09
K881862	Thermo Body Wrap Systems, Inc.	THERMO-BODY-WRAP SYSTEM	1988-10-13

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3009557417. Last updated year: 2026. Please use registration number 3009557417 when referencing this establishment in official correspondence.