# Microvision, Inc.

- Location (FDA's records): Seabrook, NH
- FDA decisions: 4 (1998–2003): 4 510(k) clearances
- Names in FDA's records: Microvision, Inc. (3); Microvision Incorporated (1)
- Product codes: LXP (1), FFS (1), GCJ (1), HQX (1)
- Predicates its devices cite: 8 (0 its own); citations of its devices by later devices: 2 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Storz Instrument Co.: 2 (https://510kreport.com/company/storz-instrument)
- Advanced Surgical Products, Inc.: 1 (https://510kreport.com/company/advanced-surgical-products)
- Vista Medical Technologies, Inc.: 1 (https://510kreport.com/company/vista-medical-technologies)
- Medivision Endoscopy: 1 (https://510kreport.com/company/medivision-endoscopy)
- Mira, Inc.: 1 (https://510kreport.com/company/mira)
- Storz Ophthalmics, Inc.: 1 (https://510kreport.com/company/storz-ophthalmics)
- Labtician Products, Inc.: 1 (https://510kreport.com/company/labtician-products)

## Firms that cite its devices most
- Ophthalmed, LLC: 1 (https://510kreport.com/company/ophthalmed)
- The Microoptical Corporation: 1 (https://510kreport.com/company/microoptical)

## Its most-cited devices
- K982462: Fiber Optic Endoillumination Probe (1998), cited by 1
- K030940: Nomad ND1000M Augmented Vision System (2003), cited by 1

## Recent decisions
- K030940: Nomad ND1000M Augmented Vision System (Apr 9, 2003)
- K022186: Scleral Plugs, 19 and 20 Gauge (Feb 26, 2003)
- K023481: Microvision Scleral Buckling Components (Jan 8, 2003)
- K982462: Fiber Optic Endoillumination Probe (Sep 14, 1998)

Source page: https://510kreport.com/company/microvision