Data / Medical devices / Switzerland / Nouvag AG
Nouvag AG: FDA-registered device maker in GOLDACH Sankt Gallen, Switzerland, 5 510(k) clearances
Nouvag AG is registered with the FDA (registration 9680741) in GOLDACH Sankt Gallen, Switzerland. It lists 17 device types. The FDA files 5 510(k) clearances under its listings, the newest dated September 5, 2026. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 9680741
- FEI number
- 3005601686
- Address
- ST. Gallerstrasse 25, GOLDACH Sankt Gallen, Switzerland, 9403
- Owner or operator
- NOUVAG AG (9008454)
- Roles
- Exporter to the US, Foreign private label distributor, Manufacturer
- First device listed
- August 12, 2004
- Registered through
- 2026
- Brand names listed
- Blades for dermatome and mucotome, Burr, drill general surgery, CHP Handpiece, Clip for external cooling, Clip for internal cooling, Contra angle, Craniotom drill, Dermatome and more
Devices it lists
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 |
|---|---|---|---|---|---|---|
| September 5, 2026 | K254135 | LipoSurg ARTIST | QPB | Substantially Equivalent | NOUVAG AG | accessdata.fda.gov |
| November 26, 2007 | K071588 | DISPENSER DP 20 | FRN | Substantially Equivalent | NOUVAG AG | accessdata.fda.gov |
| December 17, 2004 | K042943 | NOUVAG AG - VACUSON 40 AND VACUSON 60 | BTA | Substantially Equivalent | NOUVAG AG | accessdata.fda.gov |
| November 3, 2004 | K042434 | MICRO-MOTORSYSTEMS MD20, SEM2, HIGHSURG 20 & DT55 | DZI | Substantially Equivalent | NOUVAG AG | accessdata.fda.gov |
| October 1, 2003 | K022505 | CONTRA-ANGLE, MODELS 1059, 5050, 5051, 5055, 5056, 5057, 5059, 5060, 5061, 5062, 5063, 5064, 5065, 5066, 5067, 5068, | EGS | Substantially Equivalent | NOUVAG AG | accessdata.fda.gov |
Compare with other makers
- All makers of Instrument, Surgical, Orthopedic, Ac-Powered Motor And Accessory/Attachment
- All makers of Pump, Portable, Aspiration (Manual Or Powered)
- All makers of Drills, Burrs, Trephines & Accessories (Simple, Powered)
- All makers of Drill, Bone, Powered
- All makers of Drill, Surgical, Ent (Electric Or Pneumatic) Including Handpiece
- All makers of Motor, Drill, Electric
Updated September 5, 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.