Home › Device types › LZP
Aid, Surgical, Viscoelastic
FDA product code LZP · Class 3 · Ophthalmic
54
Registered devices
2,822
Adverse events
25
Recalls
0
510(k) clearances
Devices with this code
Signature — Materialise NVBiolon — AMRING PHARMACEUTICALS INC.HEALON GV PRO — JOHNSON & JOHNSON SURGICAL VISION, INC.Occucoat — Bausch & Lomb IncorporatedCELLUGEL — Alcon Laboratories, Inc.HEALON DUET PRO II — JOHNSON & JOHNSON SURGICAL VISION, INC.StableVisc — Bausch & Lomb IncorporatedPROVISC — Alcon Laboratories, Inc.DUOVISC — Alcon Laboratories, Inc.PROVISC — Alcon Laboratories, Inc.HEALON5 PRO — JOHNSON & JOHNSON SURGICAL VISION, INC.HEALON PRO — JOHNSON & JOHNSON SURGICAL VISION, INC.HEALON GV PRO — JOHNSON & JOHNSON SURGICAL VISION, INC.DUOVISC — Alcon Laboratories, Inc.VISCOAT — Alcon Laboratories, Inc.Anikavisc — Anika Therapeutics, Inc.Precision Lens Ophthalmic — Anika Therapeutics, Inc.DUOVISC — Alcon Laboratories, Inc.HEALON ENDOCOAT — JOHNSON & JOHNSON SURGICAL VISION, INC.VISCOAT — Alcon Laboratories, Inc.Anikavisc — Anika Therapeutics, Inc.HEALON DUET — JOHNSON & JOHNSON SURGICAL VISION, INC.UTF Hip Stem — UNITED ORTHOPEDIC CORP.HEALON5 PRO — JOHNSON & JOHNSON SURGICAL VISION, INC.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2026-07-31 | Johnson & Johnson Surgical Vision, Inc. | Surgical instructions sent for viscoelastic products used during ophthalmic viscosurgical cataract procedures including in part: If resistance is encountered du |
| 2019-12-03 | Johnson & Johnson Surgical Vision Inc | Ophthalmic viscosurgical device may be difficult to remove from the eye, leading to increased postoperative intraocular pressure requiring additional interventi |
| 2017-04-01 | Abbott Medical Optics Inc. (AMO) | Remote possibility that certain solutions in these lots may contain microscopic glass particles due to damage that occurred at the cylinder neck during the manu |
| 2017-04-01 | Abbott Medical Optics Inc. (AMO) | Remote possibility that certain solutions in these lots may contain microscopic glass particles due to damage that occurred at the cylinder neck during the manu |
| 2017-04-01 | Abbott Medical Optics Inc. (AMO) | Remote possibility that certain solutions in these lots may contain microscopic glass particles due to damage that occurred at the cylinder neck during the manu |
| 2017-04-01 | Abbott Medical Optics Inc. (AMO) | Remote possibility that certain solutions in these lots may contain microscopic glass particles due to damage that occurred at the cylinder neck during the manu |
| 2017-04-01 | Abbott Medical Optics Inc. (AMO) | Remote possibility that certain solutions in these lots may contain microscopic glass particles due to damage that occurred at the cylinder neck during the manu |
| 2017-04-01 | Abbott Medical Optics Inc. (AMO) | Remote possibility that certain solutions in these lots may contain microscopic glass particles due to damage that occurred at the cylinder neck during the manu |
| 2014-11-06 | Abbott Medical Optics Inc (AMO) | AMO has received complaints where the finger grip dislodged while depressing the syringe plunger. The finger grip dislodgement could result in the surgeon's ha |
| 2013-11-25 | C.L.R. Medicals International, Inc. | CLR Medicals International Inc., initiated a nationwide recall of Viscocel and Viscocel Plus, in response to FDA inspection findings of deficiencies in the Qual |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsSourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.
