# Lens Dynamics, Inc.

- Location (FDA's records): Lakewood, CO
- FDA decisions: 1 (2002–2002): 1 510(k) clearance
- Product codes: HQD (1)
- Predicates its devices cite: 2 (0 its own); citations of its devices by later devices: 3 (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
- Polymer Technology Corp.: 2 (https://510kreport.com/company/polymer-technology)

## Firms that cite its devices most
- Bausch & Lomb, Inc.: 1 (https://510kreport.com/company/bausch-lomb)
- Menicon Co, Ltd.: 1 (https://510kreport.com/company/menicon)
- Contamac, Ltd.: 1 (https://510kreport.com/company/contamac)

## Its most-cited devices
- K020006: Dyna Intra-Limbal Lens (2002), cited by 3

## Recent decisions
- K020006: Dyna Intra-Limbal Lens (Mar 29, 2002)

Source page: https://510kreport.com/company/lens-dynamics