Data / Medical devices / China / Sterivic Medical Co.,ltd.
Sterivic Medical Co.,ltd.: FDA-registered device maker in ChiZhou Anhui, China, 1 510(k) clearance
Sterivic Medical Co.,ltd. is registered with the FDA (registration 3017113900) in ChiZhou Anhui, China. It lists 3 device types. The FDA files 1 510(k) clearance under its listings, the newest dated January 28, 2026. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 3017113900
- Address
- DaDuKou Economic Development Zone, ChiZhou Anhui, China, 247210
- Owner or operator
- Sterivic Medical Co.,Ltd. (10095456)
- Roles
- Exporter to the US, Manufacturer
- First device listed
- March 15, 2026
- Registered through
- 2026
- Brand names listed
- Dental Bibs, Sterilization Pouch/Roll
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Absorber, Saliva, Paper | KHR | 1 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Indicator, Physical/Chemical Sterilization Process | JOJ | 2 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Wrap, Sterilization | FRG | 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 |
|---|---|---|---|---|---|---|
| January 28, 2026 | K251347 | Sterilization Pouch/Roll | FRG | Substantially Equivalent | Sterivic Medical Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Wrap, Sterilization
- All makers of Indicator, Physical/Chemical Sterilization Process
- All makers of Absorber, Saliva, Paper
Updated January 28, 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.