Data / Medical devices / Lithuania / UAB Viltechmeda
UAB Viltechmeda: FDA-registered device maker in VILNIUS Vilniaus Apskritis, Lithuania, 1 510(k) clearance
UAB Viltechmeda is registered with the FDA (registration 9710593) in VILNIUS Vilniaus Apskritis, Lithuania. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated June 25, 2001. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 9710593
- FEI number
- 3003513491
- Address
- Mokslininku 6, VILNIUS Vilniaus Apskritis, Lithuania, LT-08412
- Owner or operator
- MOOG INC. (9045300)
- Roles
- Manufacturer, Specification developer
- First device listed
- November 20, 2007
- Registered through
- 2026
- Brand names listed
- SEP-10S PLUS, SP-12S PRO
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Pump, Infusion | FRN | 2 | Manufacturer, 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 |
|---|---|---|---|---|---|---|
| June 25, 2001 | K010937 | SEP-10S PLUS, AND SP-12S PRO. | FRN | Substantially Equivalent | Viltechmeda | accessdata.fda.gov |
Compare with other makers
Updated June 25, 2001. 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.