Known Identifiers & Locations
FEI Numbers
3029772936
Owner Operator Numbers
N/A
Locations Covered
N/A
Registered Establishments (0)
No device registration and listing records found for this entity.
510(k) Premarket Notifications (0)
No 510(k) notifications found for this entity.
FDA Recall History (2)
| Recall # |
Product Description |
Initiation Date |
Status |
Action |
| Z-0039-2026 |
CorNeat EverPatch, REF: 1036295, Permanent Tissue-Integrating Surgical Matrix, 5.0 mm x 605 mm x 100 m
Reason: Reviewed complaints have identified that conjunctival wound dehiscence may result in early exposure of the surgical patch.
|
2025-08-18 |
Open, Classified
|
View Details
|
| 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
Reason: Reviewed complaints have identified that conjunctival wound dehiscence may result in early exposure of the surgical patch.
|
2025-08-18 |
Open, Classified
|
View Details
|
Profile Disclaimer
AvaSpecs compiles public data records from the FDA database. This compiled profile does not indicate endorsement, safety, clearance, approval, or compliance status. AvaSpecs is a private search index and is not affiliated with the FDA or any government agency.