Data / Medical devices / Dominican Republic / T-Scientific International, Inc.
T-Scientific International, Inc.: FDA-registered device maker in SANTO DOMINGO Distrito Nacional, Dominican Republic, 1 510(k) clearance
T-Scientific International, Inc. is registered with the FDA (registration 3006113097) in SANTO DOMINGO Distrito Nacional, Dominican Republic. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated April 21, 2003. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3006113097
- Address
- Surgex Building Zona Franca San Isidro, SANTO DOMINGO Distrito Nacional, Dominican Republic, N/A
- Owner or operator
- T-SCIENTIFIC INTERNATIONAL, INC. (9088753)
- Roles
- Specification developer
- First device listed
- June 19, 2006
- Registered through
- 2026
- Brand names listed
- T-PAD, V-PAD
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Hemostatic Wound Dressing Without Thrombin Or Other Biologics | QSY | U | Specification developer | accessdata.fda.gov |
| Splint, Intranasal Septal | LYA | 1 | Specification developer | 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 |
|---|---|---|---|---|---|---|
| April 21, 2003 | K030334 | T-SCIENTIFIC T-PAD | QSY | Substantially Equivalent | T-Scientific, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Hemostatic Wound Dressing Without Thrombin Or Other Biologics
- All makers of Splint, Intranasal Septal
Updated April 21, 2003. 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.