Data / Medical devices / United States / Microvision, Inc.
Microvision, Inc.: FDA-registered device maker in Seabrook, NH, United States, 2 510(k) clearances
Microvision, Inc. is registered with the FDA (registration 1226011) in Seabrook, NH, United States. It lists 2 device types. The FDA files 2 510(k) clearances under its listings, the newest dated January 8, 2003. Registered through 2026. FDA data exported November 2, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- FDA registration number
- 1226011
- FEI number
- 3002532015
- Address
- 20 London Ln, Seabrook, NH, United States, 03874
- Owner or operator
- MicroVision, Inc. (9034466)
- Roles
- Manufacturer
- First device listed
- March 14, 2013
- Registered through
- 2026
- Brand names listed
- Fiber Optic Endoillumination Probe, Retinal Implants, Scleral Buckling Components
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Image, Illumination, Fiberoptic, For Endoscope | FFS | 2 | Manufacturer | accessdata.fda.gov |
| Implant, Orbital, Extra-Ocular | HQX | 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 |
|---|---|---|---|---|---|---|
| January 8, 2003 | K023481 | MICROVISION SCLERAL BUCKLING COMPONENTS | HQX | Substantially Equivalent | Microvision, Inc. | accessdata.fda.gov |
| September 14, 1998 | K982462 | FIBER OPTIC ENDOILLUMINATION PROBE | FFS | Substantially Equivalent | Microvision, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Implant, Orbital, Extra-Ocular
- All makers of Image, Illumination, Fiberoptic, For Endoscope
Updated January 8, 2003. 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.