Sleepnet Corporation is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Sleepnet Corporation - FDA 510(k) Cleared Devices
Recent clearances: Sleepnet Arie Full Face Vented Mask, Mojo Full Face Vented Mask, Mojo Full Face Non-Vented Mask
23
Total
23
Cleared
0
Denied
Sleepnet Corporation has 23 FDA 510(k) cleared anesthesiology devices. Based in Manchester, US.
Latest FDA clearance: Jan 2026. Active since 1996.
Browse the complete list of FDA 510(k) cleared anesthesiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Sleepnet Corporation % Promedic, LLC, ProMedic, LLC and ProMedic Consulting, LLC.
FDA 510(k) Regulatory Record - Sleepnet Corporation
23 devices
Cleared
Jan 15, 2026
Sleepnet Arie Full Face Vented Mask
Anesthesiology
213d
Cleared
Oct 18, 2024
Mojo Full Face Vented Mask
Anesthesiology
116d
Cleared
Aug 28, 2024
Mojo Full Face Non-Vented Mask
Anesthesiology
57d
Cleared
Jul 10, 2024
Mojo 2 Full Face Vented Mask
Anesthesiology
30d
Cleared
Jun 27, 2024
Mojo 2 Full Face Non-Vented Mask
Anesthesiology
29d
Cleared
Jun 15, 2024
iQ 2 Nasal Vented Mask
Anesthesiology
22d
Cleared
Jan 10, 2022
iQ 2 Nasal Mask, Phantom 2 Nasal Mask
Anesthesiology
258d
Cleared
Apr 30, 2021
Innova Nasal Non-Vented Mask
Anesthesiology
142d
Cleared
Jul 26, 2019
Mojo 2 Full Face Non-Vented Mask, Mojo 2 AAV Non-Vented Full-Face Mask,...
Anesthesiology
144d
Cleared
Jul 05, 2019
Mojo 2 Full Face Vented Mask, Veraseal 3 Full Face Vented Mask, V3 Full Face...
Anesthesiology
148d
Cleared
Nov 30, 2012
HARD SHELL VENTED NASAL MASK
Anesthesiology
212d
Cleared
Nov 05, 2012
MINIME 2 NASAL MASK
Anesthesiology
151d