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.
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