Data / Medical devices / China / Bestway Plastic And Metal Products Ltd.
Bestway Plastic And Metal Products Ltd.: FDA-registered device maker in Dongguan Guangdong, China, 1 510(k) clearance
Bestway Plastic And Metal Products Ltd. is registered with the FDA (registration 3039435282) in Dongguan Guangdong, China. It lists 13 device types. The FDA files 1 510(k) clearance under its listings, the newest dated June 15, 2025. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 3039435282
- Address
- Room 701, Building 2, No.1 Chuangye San Road, Mapu Ao, Fenggang Town, Dongguan Guangdong, China, 523682
- Owner or operator
- Bestway Plastic And Metal Products Ltd. (10093721)
- Roles
- Manufacturer
- First device listed
- June 27, 2025
- Registered through
- 2026
- Brand names listed
- Air humidifer, Model: BJS-01,BJS-02,BJS-03,BJS-04,BJS-05,BJS-06,BJS-07,BJS-08,BJS-09,BJS-10, Automatic Soap dispenser, Model: BZY-01/BZY-02/BZY-03/BZY-04/BZY-05/BZY-06/BZY-07/BZY-08/BZY-09/BZY-10, Car air purifer, Model: BCAP-01/BCAP-02/BCAP-03/BCAP-04/BCAP-05/BCAP-06/BCAP-07/BCAP-08/BCAP-09/BCAP-10, Car charger purifier, Model: BC-01/BC-02/BC-03/BC-04/BC-05/BC-06/BC-07/BC-08/BC-09/BC-10, Electric eyebrow trimmer, Model: BET-01/BET-02/BET-03/BET-04/BET-05/BET-06/BET-07/BET-08/BET-09/BET-10, Eye massager, Model: BEM-01/BEM-02/BEM-03/BEM-04/BEM-05/BEM-06/BEM-07/BEM-08/BEM-09/BEM-10, Facial sprayer, Model: BSP-01/BSP-02/BSP-03/BSP-04/BSP-05/BSP-06/BSP-07/BSP-08/BSP-09/BSP-10, Facial steamer, Model: BFS-01/BFS-02/BFS-03/BFS-04/BFS-05/BFS-06/BFS-07/BFS-08/BFS-09/BFS-10 and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Brush, Dermabrasion, Powered | GFE | 1 | Manufacturer | accessdata.fda.gov |
| Device, Pressure Applying | KNM | 1 | Manufacturer | accessdata.fda.gov |
| Disinfectant, Medical Devices | LRJ | 1 | Manufacturer | accessdata.fda.gov |
| Dispenser, Liquid Medication | KYX | 1 | Manufacturer | accessdata.fda.gov |
| Epilator, High Frequency, Needle-Type | KCW | 1 | Manufacturer | accessdata.fda.gov |
| Humidifier, Non-Direct Patient Interface (Home-Use) | KFZ | 1 | Manufacturer | accessdata.fda.gov |
| Lamp, Infrared, Therapeutic Heating | ILY | 2 | Manufacturer | accessdata.fda.gov |
| Light Based Over-The-Counter Hair Removal | OHT | 2 | Manufacturer | accessdata.fda.gov |
| Massager, Therapeutic, Electric | ISA | 1 | Manufacturer | accessdata.fda.gov |
| Massager, Therapeutic, Manual | LYG | 1 | Manufacturer | accessdata.fda.gov |
| Mirror, Ent | KAI | 1 | Manufacturer | accessdata.fda.gov |
| Support, Head, Surgical, Ent | EPW | 1 | Manufacturer | accessdata.fda.gov |
| Unit, Oral Irrigation | EFS | 1 | 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 |
|---|---|---|---|---|---|---|
| June 15, 2025 | K243036 | IPL Hair Removal Device (BHRL-01, BHRL-02, BHRL-03, BHRL-04, BHRL-05, BHRL-06, BHRL-06B, BHRL-07, BHRL-08, BHRL-09, BHRL-10, BHRL-11, BHRL-12, BHRL-13, BHRL-14, BHRL-15, BHRL-16, BHRL-17, BHRL-18, BHRL-19, BHRL-20, BHRL-21, BHRL-22, BHRL-23, BHRL-24, BHRL-25, BHRL-26, BHRL-27, BHRL-28, BHRL-29) | OHT | Substantially Equivalent | Bestway Plastic and Metal Products , Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Lamp, Infrared, Therapeutic Heating
- All makers of Mirror, Ent
- All makers of Light Based Over-The-Counter Hair Removal
- All makers of Dispenser, Liquid Medication
- All makers of Disinfectant, Medical Devices
- All makers of Support, Head, Surgical, Ent
Updated June 15, 2025. 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.