Data / Medical devices / Switzerland / Alcon Grieshaber AG
Alcon Grieshaber AG: FDA-registered device maker in Neuhausen Schaffhausen, Switzerland, 2 510(k) clearances
Alcon Grieshaber AG is registered with the FDA (registration 3033485955) in Neuhausen Schaffhausen, Switzerland. It lists 12 device types. The FDA files 2 510(k) clearances under its listings, the newest dated November 12, 2010. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3033485955
- Address
- Victor von Bruns-Strasse 21, Neuhausen Schaffhausen, Switzerland, 8212
- Owner or operator
- Alcon Laboratories, Inc. (1610287)
- Roles
- Specification developer
- First device listed
- December 30, 1977
- Registered through
- 2026
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Apparatus, Cautery, Radiofrequency, Ac-Powered | HQR | 2 | Specification developer | accessdata.fda.gov |
| Cannula, Ophthalmic | HMX | 1 | Specification developer | accessdata.fda.gov |
| Cannula, Trocar, Ophthalmic | NGY | 1 | Specification developer | accessdata.fda.gov |
| Clip, Iris Retractor | HOC | 1 | Specification developer | accessdata.fda.gov |
| Forceps, Ophthalmic | HNR | 1 | Specification developer | accessdata.fda.gov |
| Hook, Ophthalmic | HNQ | 1 | Specification developer | accessdata.fda.gov |
| Knife, Ophthalmic | HNN | 1 | Specification developer | accessdata.fda.gov |
| Lens, Fundus, Hruby, Diagnostic | HJI | 1 | Specification developer | accessdata.fda.gov |
| Scissors, Ophthalmic | HNF | 1 | Specification developer | accessdata.fda.gov |
| Spatula, Ophthalmic | HND | 1 | Specification developer | accessdata.fda.gov |
| Unit, Phacofragmentation | HQC | 2 | Specification developer | accessdata.fda.gov |
| Vitrectomy, Instrument Cutter | MLZ | 2 | 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 12, 2010 | K101285 | CONSTELLATION VISION SYSTEM | HQC | Substantially Equivalent | Alcon Manufacturing, Ltd. | accessdata.fda.gov |
| July 2, 2002 | K021566 | INFINITI | HQC | Substantially Equivalent | Alcon Laboratories, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Unit, Phacofragmentation
- All makers of Vitrectomy, Instrument Cutter
- All makers of Apparatus, Cautery, Radiofrequency, Ac-Powered
- All makers of Cannula, Ophthalmic
- All makers of Forceps, Ophthalmic
- All makers of Scissors, Ophthalmic
Updated November 12, 2010. 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.