Data / Medical devices / Switzerland / Oscimed SA
Oscimed SA: FDA-registered device maker in LA CHAUX-DE-FONDS, NE Neuchatel, Switzerland, 1 510(k) clearance
Oscimed SA is registered with the FDA (registration 9614473) in LA CHAUX-DE-FONDS, NE Neuchatel, Switzerland. It lists 3 device types. The FDA files 1 510(k) clearance under its listings, the newest dated January 16, 2024. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 9614473
- FEI number
- 3003767844
- Address
- Fritz-Courvoisier 105, LA CHAUX-DE-FONDS, NE Neuchatel, Switzerland, 2300
- Owner or operator
- Oscimed SA (9038103)
- Roles
- Manufacturer
- First device listed
- June 1, 1999
- Registered through
- 2026
- Brand names listed
- Anti-snore Mouth Guard+, ORTHOPEDIC VACUUM CLEANER FOR OSCIMED PLASTER SAWS, PLASTER SAW OSCIMED PSV, PLASTER SAW OSCIMED PSV II
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Device, Anti-Snoring | LRK | 2 | Manufacturer | accessdata.fda.gov |
| Dilator, Nasal | LWF | 1 | Manufacturer | accessdata.fda.gov |
| Instrument, Cast Removal, Ac-Powered | LGH | 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 16, 2024 | K231138 | Aniti-Snore Mouthguard+ | LRK | Substantially Equivalent | Oscimed SA | accessdata.fda.gov |
Compare with other makers
- All makers of Instrument, Cast Removal, Ac-Powered
- All makers of Dilator, Nasal
- All makers of Device, Anti-Snoring
Updated January 16, 2024. 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.