Alafair Biosciences, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Alafair Biosciences, Inc. - FDA 510(k) Cleared Devices
Recent clearances: VersaWrap, VersaWrap Nerve Protector, VersaWrap
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.
510(k) submissions have been managed by Namsa as regulatory consultant.
FDA 510(k) Regulatory Record - 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