# Summit Technology, Inc.

- Location (FDA's records): Waltham, MA
- FDA decisions: 5 (1990–1998): 5 510(k) clearances
- Product codes: EQH (2), HQF (1), GEX (1), HNO (1)
- Predicates its devices cite: 1 (0 its own); citations of its devices by later devices: 1 (0 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Eyetech M.V.A.: 1 (https://510kreport.com/company/eyetech-mva)

## Firms that cite its devices most
- Bkg Opthalmics USA, Inc.: 1 (https://510kreport.com/company/bkg-opthalmics-usa)

## Its most-cited devices
- K980675: Summit Krumeich-Barraquer Microkeratome (1998), cited by 1

## Recent decisions
- K980675: Summit Krumeich-Barraquer Microkeratome (Dec 22, 1998)
- K926470: Laser and Emphasis Sclerostomy Tip (Jul 22, 1993)
- K915651: Omnimed Holmium Laser and Delivery System (Jun 15, 1992)
- K912522: Omniview (TM) Ophthalmic Fiberendo W/Needleholder (Jul 25, 1991)
- K904470: Summit Tech 19/20 Gauge Ophthalmic Fiberendoscope (Dec 24, 1990)

Source page: https://510kreport.com/company/summit-technology