Data / Medical devices / China / Mima-Pro (nan Tong) Scientific Inc.
Mima-Pro (nan Tong) Scientific Inc.: FDA-registered device maker in Nantong Jiangsu, China, 1 510(k) clearance
Mima-Pro (nan Tong) Scientific Inc. is registered with the FDA (registration 3027728071) in Nantong Jiangsu, China. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated February 28, 2023. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 3027728071
- Address
- Bld 8, Boding Machinery Industrial Park Xingyuan Road, Tongzhou District, Nantong Jiangsu, China, 226300
- Owner or operator
- Mima-Pro (Nan Tong) Scientific Inc. (10088532)
- Roles
- Manufacturer
- First device listed
- August 9, 2023
- Registered through
- 2027
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| System, Ablation, Microwave And Accessories | NEY | 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 |
|---|---|---|---|---|---|---|
| February 28, 2023 | K223272 | SurBlate Ablation System | NEY | Substantially Equivalent | Mima-Pro Scientific, Inc. | accessdata.fda.gov |
Compare with other makers
Updated February 28, 2023. 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.