Data / Medical devices / China / Wenzhou Lingfeng Electronic Technology Co., Ltd
Wenzhou Lingfeng Electronic Technology Co., Ltd: FDA-registered device maker in Ruian Zhejiang, China, 2 510(k) clearances
Wenzhou Lingfeng Electronic Technology Co., Ltd is registered with the FDA (registration 3009557417) in Ruian Zhejiang, China. It lists 4 device types. The FDA files 2 510(k) clearances under its listings, the newest dated May 5, 2026. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3009557417
- Address
- No.6 Puxi Industry Zone, Tongpu, Ruian Zhejiang, China, 325216
- Owner or operator
- WENZHOU LINGFENG ELECTRONIC TECHNOLOGY CO., LTD (10040198)
- Roles
- Complaint file establishment, Exporter to the US, Manufacturer
- First device listed
- March 18, 2012
- Registered through
- 2026
- Brand names listed
- 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., 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, 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 AI01.AI02.AI03.AI04.AI05.AI06, Air Compression Massager models BG01.BG02.BG03.BG04.BG05.BG06, Air Compression Massager models LF-FT001.LF-FT002.LF-FT003.LF-FT004.LF-FT005.LF-FT006, 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 LF001.LF002.LF003.LF004.LF005.LF006 and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Massager, Powered Inflatable Tube | IRP | 2 | Complaint file establishment, Manufacturer | accessdata.fda.gov |
| Massager, Therapeutic, Electric | ISA | 1 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Pad, Heating, Powered | IRT | 2 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Vibrator, Therapeutic | IRO | 1 | Exporter to the US, Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| May 5, 2026 | K254200 | 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, 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, 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, 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) | IRP | Substantially Equivalent | Wenzhou Lingfeng Electronic Technology Co., Ltd. | accessdata.fda.gov |
| November 15, 2021 | K213000 | Air Compression Massager (Model LF-FT003) | IRP | Substantially Equivalent | Wenzhou Lingfeng Electronic Technology Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Massager, Therapeutic, Electric
- All makers of Vibrator, Therapeutic
- All makers of Massager, Powered Inflatable Tube
- All makers of Pad, Heating, Powered
Updated May 5, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.