Data / Medical devices / United States / Ocusciences, Inc.
Ocusciences, Inc.: FDA-registered device maker in Ann Arbor, MI, United States, 1 510(k) clearance
Ocusciences, Inc. is registered with the FDA (registration 3017133887) in Ann Arbor, MI, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated April 22, 2025. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3017133887
- Address
- 2890 Carpenter Rd Ste 1800, Ann Arbor, MI, United States, 48108
- Owner or operator
- OcuSciences, Inc. (10093572)
- Roles
- Manufacturer
- First device listed
- June 9, 2025
- Registered through
- 2026
- Brand names listed
- Ocumet Beacon
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Ophthalmoscope, Laser, Scanning | MYC | 2 | 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 |
|---|---|---|---|---|---|---|
| April 22, 2025 | K241931 | OcuMet Beacon (OCUB100) | MYC | Substantially Equivalent | Ocusciences, Inc. | accessdata.fda.gov |
Compare with other makers
Updated April 22, 2025. 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.