Data / Medical devices / China / FDC Technology Industry Company
FDC Technology Industry Company: FDA-registered device maker in Taishan,GUANG CHONG Guangdong, China, 1 510(k) clearance
FDC Technology Industry Company is registered with the FDA (registration 3005938413) in Taishan,GUANG CHONG Guangdong, China. It lists 6 device types. The FDA files 1 510(k) clearance under its listings, the newest dated January 27, 2025. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 3005938413
- Address
- No. 2 INDUSTRIAL DISTRICT SHAGONG HU, Taishan,GUANG CHONG Guangdong, China, 529200
- Owner or operator
- Firstar Dental Company (10032605)
- Roles
- Exporter to the US, Manufacturer
- First device listed
- May 28, 2010
- Registered through
- 2026
- Brand names listed
- Firstar Cabinet Mounted Dental Unit, Firstar Cart Mounted Dental Unit, Firstar Chair Mounted Dental Unit, Firstar Wall Mounted Dental Unit
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Chair, Dental, Without Operative Unit | NRU | 1 | Manufacturer | accessdata.fda.gov |
| Light, Operating, Dental | EAZ | 1 | Manufacturer | accessdata.fda.gov |
| Unit, Operative Dental | EIA | 1 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Unit, Operative Dental, Accessories | NRD | 1 | Manufacturer | accessdata.fda.gov |
| Unit, Suction Operatory | EBR | 1 | Manufacturer | accessdata.fda.gov |
| Unit, Syringe, Air And/Or Water | ECB | 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 |
|---|---|---|---|---|---|---|
| January 27, 2025 | K231297 | Firstar Dental Unit | EIA | Substantially Equivalent | Firstar Dental Company | accessdata.fda.gov |
Compare with other makers
- All makers of Unit, Suction Operatory
- All makers of Light, Operating, Dental
- All makers of Unit, Operative Dental
- All makers of Chair, Dental, Without Operative Unit
- All makers of Unit, Operative Dental, Accessories
- All makers of Unit, Syringe, Air And/Or Water
Updated January 27, 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.