Data / Medical devices / China / Fujian Tonggang Industries Ltd.
Fujian Tonggang Industries Ltd.: FDA-registered device maker in Quanzhou Fujian, China, 1 510(k) clearance
Fujian Tonggang Industries Ltd. is registered with the FDA (registration 3030534974) in Quanzhou Fujian, China. It lists 6 device types. The FDA files 1 510(k) clearance under its listings, the newest dated August 13, 2025. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3030534974
- Address
- Unit 06, 14th Floor, Block B, Puxi Wanda Plaza, Fengze District, Quanzhou Fujian, China, 362000
- Owner or operator
- FuJian TongGang Industries Ltd. (10089814)
- Roles
- Exporter to the US, Manufacturer
- First device listed
- January 10, 2024
- Registered through
- 2026
- Brand names listed
- Tampons, Unscented menstrual Cardboard Applicator Tampons;, Unscented menstrual Digital Tampons;, Unscented menstrual long applicator tampons;, baby nappies,baby diapers, baby pull-up pants, incontinence pads, adult nappies, adult diapers,adult pull-up pants,, baby wipes, adult wipes, pet wipes, face masks, KN95 face masks, menstrual pants and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Disinfectant, Medical Devices | LRJ | 1 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Face Mask Within The Scope Of The Face Mask And Barrier Face Covering Enforcement Policy Or Face Mask Umbrella Eua | QKR | N | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Garment, Protective, For Incontinence | EYQ | 1 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Nursing Pad, Polyurethane Pad With Starch Copolymer, Glycerin, And Surfactant (F-68) | NTX | 1 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Pad, Menstrual, Unscented | HHD | 1 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Tampon, Menstrual, Unscented | HEB | 2 | 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 |
|---|---|---|---|---|---|---|
| August 13, 2025 | K251033 | Unscented menstrual long applicator tampon; Unscented menstrual Compact Applicator Tampon; Unscented menstrual Cardboard Applicator Tampon; Unscented menstrual Digital Tampons | HEB | Substantially Equivalent | Unibeauty (Hubei) Technology Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Nursing Pad, Polyurethane Pad With Starch Copolymer, Glycerin, And Surfactant (F-68)
- All makers of Tampon, Menstrual, Unscented
- All makers of Disinfectant, Medical Devices
- All makers of Face Mask Within The Scope Of The Face Mask And Barrier Face Covering Enforcement Policy Or Face Mask Umbrella Eua
- All makers of Garment, Protective, For Incontinence
- All makers of Pad, Menstrual, Unscented
Updated August 13, 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.