Kerecis Limited - FDA 510(k) Cleared Devices
10
Total
10
Cleared
0
Denied
Kerecis Limited has 10 FDA 510(k) cleared general & plastic surgery devices. Based in Isafjordur, IS.
Latest FDA clearance: Jul 2025. Active since 2013.
Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Kerecis Limited
10 devices
Cleared
Jul 16, 2025
Marigen Wound Extra
General & Plastic Surgery
30d
Cleared
Jul 15, 2025
Kerecis SurgiBind (50241)
General & Plastic Surgery
29d
Cleared
Jun 04, 2025
Tendon Protect (50242)
Orthopedic
173d
Cleared
Aug 21, 2024
Kerecis Parvus (50207)
General & Plastic Surgery
124d
Cleared
Jun 29, 2022
Kerecis Silicone
General & Plastic Surgery
272d
Cleared
May 02, 2021
Kerecis Reconstruct
General & Plastic Surgery
250d
Cleared
Nov 13, 2020
Kerecis Gingiva Graft
Dental
420d
Cleared
Jul 10, 2019
MariGen Wound Extra
General & Plastic Surgery
128d
Cleared
Aug 19, 2016
Kerecis SecureMesh
General & Plastic Surgery
273d
Cleared
Oct 23, 2013
MARIGEN WOUND DRESSING
General & Plastic Surgery
85d