# Opti-Centre Laboratories

- Location (FDA's records): Grand Junction, CO
- FDA decisions: 6 (1998–2005): 6 510(k) clearances
- Product codes: LPL (6)
- Predicates its devices cite: 3 (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
- Benz Research and Development Corp.: 3 (https://510kreport.com/company/benz-research-and-development)

## Firms that cite its devices most
- X-Cel Contacts, Inc.: 1 (https://510kreport.com/company/x-cel-contacts)
- CooperVision, Inc.: 1 (https://510kreport.com/company/coopervision)

## Its most-cited devices
- K043129: Proclear Ultravue Multifocal and Proclear Ultravue 2000T Multifocal Toric (Omaflicon a) Soft (Hydrophilic Contact Lens) (2005), cited by 2

## Recent decisions
- K043129: Proclear Ultravue Multifocal and Proclear Ultravue 2000T Multifocal Toric (Omaflicon a) Soft (Hydrophilic Contact Lens) (Jan 12, 2005)
- K010256: Ultravue/P 2000T, Ultravue/C 2000T (Hioxifilcon B) Soft (Multifocal Toric) Daily Wear Contact Lens (Clear & Blue Visibil (Mar 26, 2001)
- K001227: Ultra Vue 55/P & C (Methafilcon a) Soft (Multifocal, Spherical, & Toric) Daily Wear Contact Lens (Clear & Blue Visibilit (Jun 29, 2000)
- K992589: Resolution 5X (Spherical) and Ultra Gel 5X (Toric)(Hioxifilcon a) Soft Daily Wear Contact Lens, (Clear & Blue Visibility (Aug 26, 1999)
- K983496: Resolution 45 (Spherical) and Ultra Gel (Toric) (Hioxifilcon B) Soft Daily Wear Contact Lens, )Clear & Blue Visibility T (Mar 29, 1999)
- K974599: Ultravue/P, Ultralvue/C (Hioxifilcon B)) Soft (Multifocal) Daily Wear Contact Lens (Clear & Yinted, Lathe-Cut From Lens) (Mar 2, 1998)

Source page: https://510kreport.com/company/opti-centre-laboratories