# X-Cel Contacts, Inc.

- Location (FDA's records): Grand Junction, CO
- FDA decisions: 2 (2007–2010): 2 510(k) clearances
- Names in FDA's records: X-Cel Contacts, Inc. (1); X-Cel Contacts (1)
- Product codes: LPL (2)
- Predicates its devices cite: 7 (1 its own); citations of its devices by later devices: 2 (1 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
- Art Optical Contact Lens, Inc.: 1 (https://510kreport.com/company/art-optical-contact-lens)
- CooperVision, Inc.: 1 (https://510kreport.com/company/coopervision)
- Hydron, Ltd.: 1 (https://510kreport.com/company/hydron)
- Opti-Centre Laboratories: 1 (https://510kreport.com/company/opti-centre-laboratories)
- Westcon Contact Lens Co., Inc.: 1 (https://510kreport.com/company/westcon-contact-lens)
- Les Laboratoires Blanchard: 1 (https://510kreport.com/company/les-laboratoires-blanchard)

## Firms that cite its devices most
- X-Cel Specialty Contacts, A Walman Optical Company: 1 (https://510kreport.com/company/x-cel-specialty-contacts-a-walman-optical)

## Its most-cited devices
- K100443: Definitive, Flexlens - Silicone Hydrogel (2010), cited by 1
- K070308: Flexlens Multifocal Soft Contact Lens, (Hioxifilcon a) and (Hioxifilcon B) for Daily Wear (2007), cited by 1

## Recent decisions
- K100443: Definitive, Flexlens - Silicone Hydrogel (Oct 28, 2010)
- K070308: Flexlens Multifocal Soft Contact Lens, (Hioxifilcon a) and (Hioxifilcon B) for Daily Wear (Mar 12, 2007)

Source page: https://510kreport.com/company/x-cel-contacts