Corneat Vision , Ltd.
Corneat Vision , Ltd. holds FDA 510(k) medical device clearance, cleared in 2023, with 3 FDA device recalls on record.
Top product codes for Corneat Vision , Ltd.
FDA recalls by Corneat Vision , Ltd.
- Z-0039-2026 — CorNeat EverPatch, REF: 1036295, Permanent Tissue-Integrating Surgical Matrix, 5.0 mm x 605 mm x 100 ¿m
- Z-0040-2026 — EverPatch+, REF: 1044002, Permanent Scleral Reinforcement Matrix 1x5.0mm x 8.5 mm Shield/1 x 5.0mm x 6.5 mm Rectangle, STERILE VH202
- Z-2537-2025 — CorNeat EverPatch, REF: 1036295, Permanent Tissue-Integrating Surgical Matrix, 5.0 mm x 6.5 mm x 100 um, SterileEO, RX only
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Corneat Vision , Ltd.
Data sourced from openFDA. This site is unofficial and independent of the FDA.