Data / Medical devices / China / Foshan Haiseer Electronic Technology Co., Ltd.
Foshan Haiseer Electronic Technology Co., Ltd.: FDA-registered device maker in Foshan Guangdong, China, 1 510(k) clearance
Foshan Haiseer Electronic Technology Co., Ltd. is registered with the FDA (registration 3043729119) in Foshan Guangdong, China. It lists 6 device types. The FDA files 1 510(k) clearance under its listings, the newest dated May 10, 2021. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3043729119
- Address
- Room 701-1, Building 3, Youchuang Intelligent Manufacturing Park No. 9 Libo Road, Shishan Town, Nanhai District, Foshan Guangdong, China, 528000
- Owner or operator
- Foshan Haiseer Electronic Technology Co., Ltd. (10095184)
- Roles
- Manufacturer
- First device listed
- February 4, 2026
- Registered through
- 2026
- Brand names listed
- Diode Laser Therapy Systems, EPM Microcrystal Introduction Instrument, Female External Catheter for Powered Urine Collection System, Male External Catheter for Powered Urine Collection System, Nasal Bandage / Post-Surgery Nasal Bandage With Cotton Pad, PZHZ External Urine Collection System (M-S01, M-01, F-01), Red light machine, Therapeutic Chiropractic Massager, Model: 3068, Yowelcom Male External Catheter, Tansheep Male External Catheter
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Bandage, Elastic | FQM | 1 | Manufacturer | accessdata.fda.gov |
| Brush, Dermabrasion, Powered | GFE | 1 | Manufacturer | accessdata.fda.gov |
| Collector, Urine, Powered, Non Indwelling Catheter | NZU | 1 | Manufacturer | accessdata.fda.gov |
| Lamp, Infrared, Therapeutic Heating | ILY | 2 | Manufacturer | accessdata.fda.gov |
| Massager, Therapeutic, Electric | ISA | 1 | Manufacturer | accessdata.fda.gov |
| Powered Laser Surgical Instrument | GEX | 2 | 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 10, 2021 | K210168 | Diode Laser Therapy Systems | GEX | Substantially Equivalent | Beijing Kes Biology Technology Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Powered Laser Surgical Instrument
- All makers of Collector, Urine, Powered, Non Indwelling Catheter
- All makers of Bandage, Elastic
- All makers of Massager, Therapeutic, Electric
- All makers of Brush, Dermabrasion, Powered
- All makers of Lamp, Infrared, Therapeutic Heating
Updated May 10, 2021. 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.