Deka Research and Development is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Deka Research and Development - FDA 510(k) Cleared Devices
Recent clearances: iiSure Infusion Set, Sparta Infusion Set for Insulin, HemoCare Hemodialysis System
13
Total
13
Cleared
0
Denied
Deka Research and Development has 13 FDA 510(k) cleared medical devices. Based in Manchester, US.
Latest FDA clearance: Jun 2026. Active since 2015. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Deka Research and Development Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Deka Research and Development
13 devices
Cleared
Jun 17, 2026
twiist Automated Insulin Delivery (AID) System
Chemistry
27d
Cleared
Jun 03, 2026
iiSure Infusion Set
Chemistry
26d
Cleared
Aug 01, 2025
Sparta Infusion Set for Insulin
Chemistry
231d
Cleared
Jul 12, 2024
HemoCare Hemodialysis System
Gastroenterology & Urology
249d
Cleared
Jul 12, 2024
HemoCare Bicarbonate Concentrate Set (BCS)
Gastroenterology & Urology
99d
Cleared
Jun 12, 2024
Remunity System
General Hospital
133d
Cleared
May 24, 2024
DEKA ACE Pump System
Chemistry
25d
Cleared
Mar 13, 2024
DEKA ACE Pump System
Chemistry
89d
Cleared
Mar 13, 2024
DEKA Loop
Chemistry
82d
Cleared
Mar 01, 2024
DEKA Infusion System, DEKA Administration Set
General Hospital
211d
Cleared
Jul 25, 2023
DEKA ACE Pump System
Chemistry
627d
Cleared
Dec 30, 2020
Remunity Pump for Remodulin (treprostinil) Injection
General Hospital
106d