Alafair Biosciences, Inc. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Alafair Biosciences, Inc. has 7 FDA 510(k) cleared medical devices. Based in Austin, US.
Latest FDA clearance: Jun 2024. Active since 2016. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Alafair Biosciences, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Alafair Biosciences, Inc.
7 devices
Cleared
Jun 14, 2024
VersaWrap
Orthopedic
81d
Cleared
Nov 02, 2023
VersaWrap Nerve Protector
Neurology
118d
Cleared
Oct 29, 2021
VersaWrap
General & Plastic Surgery
31d
Cleared
Mar 09, 2021
VersaWrap
General & Plastic Surgery
90d
Cleared
Sep 14, 2020
VersaWrap Nerve Protector
Neurology
90d
Cleared
Mar 06, 2020
VersaWrap Tendon Protector
General & Plastic Surgery
29d
Cleared
Jun 10, 2016
VersaWrap Tendon Protector
Orthopedic
122d