Data / Medical devices / Switzerland / APIS Technologies Sarl
APIS Technologies Sarl: FDA-registered device maker in Geneva Geneve, Switzerland, 2 510(k) clearances
APIS Technologies Sarl is registered with the FDA (registration 3017791709) in Geneva Geneve, Switzerland. It lists 2 device types. The FDA files 2 510(k) clearances under its listings, the newest dated November 7, 2006. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3017791709
- Address
- Rue De La Cite 1, Geneva Geneve, Switzerland, 1204
- Owner or operator
- CL MEDICAL (9077482)
- Roles
- Manufacturer, Specification developer
- First device listed
- September 13, 2005
- Registered through
- 2026
- Brand names listed
- I STOP FEMALE SLING, I-STOP, I-STOP TOMS, I-STOP TRANS OBTURATOR MALE SLING
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Mesh, Surgical, For Stress Urinary Incontinence, Male | OTM | 2 | Manufacturer, Specification developer | accessdata.fda.gov |
| Mesh, Surgical, Synthetic, Urogynecologic, For Stress Urinary Incontinence, Retropubic Or Transobturator | OTN | 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 |
|---|---|---|---|---|---|---|
| November 7, 2006 | K063079 | I-STOP TRANS OBTURATOR MALE SLING | OTM | Substantially Equivalent | Cl Medical | accessdata.fda.gov |
| August 11, 2005 | K051533 | I-STOP | OTN | Substantially Equivalent | Cl Medical | accessdata.fda.gov |
Compare with other makers
- All makers of Mesh, Surgical, For Stress Urinary Incontinence, Male
- All makers of Mesh, Surgical, Synthetic, Urogynecologic, For Stress Urinary Incontinence, Retropubic Or Transobturator
Updated November 7, 2006. 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.