Lens, Guide, Intraocular
FDA product code KYB · Class 1 · 10 devices · 2,264 reports · 1 devices named in recalls
- MONARCH® III 8065977763Alcon Laboratories, Inc. · LENS, GUIDE, INTRAOCULAR1 recall1,042 reports
- UNFOLDER PLATINUM 1 SERIES 1MTEC30Johnson & Johnson Surgical Vision, Inc. · LENS, GUIDE, INTRAOCULAR524 reports
- MONARCH® III 8065977773Alcon Laboratories, Inc. · LENS, GUIDE, INTRAOCULAR338 reports
- UNFOLDER EMERALD EMERALDCJohnson & Johnson Surgical Vision, Inc. · LENS, GUIDE, INTRAOCULAR250 reports
- UNFOLDER SILVER PSCSTJohnson & Johnson Surgical Vision, Inc. · LENS, GUIDE, INTRAOCULAR66 reports
- MONARCH® II 8065977758Alcon Laboratories, Inc. · LENS, GUIDE, INTRAOCULAR22 reports
- ONE SERIES ULTRA 1VIPR30Johnson & Johnson Surgical Vision, Inc. · LENS, GUIDE, INTRAOCULAR8 reports
- UNFOLDER EMERALD EMERALDTJohnson & Johnson Surgical Vision, Inc. · LENS, GUIDE, INTRAOCULAR8 reports
- Bausch + Lomb AI-28Bausch & Lomb Incorporated · Lens, Guide, Intraocular3 reports
- UNFOLDER EMERALD AR 1CART30Johnson & Johnson Surgical Vision, Inc. · LENS, GUIDE, INTRAOCULAR3 reports