Neomed, Inc. is one of 12944 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Neomed, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Oral/Enteral Syringes with ENFit connector (12 mL to 60 mL), Low Dose Tip Oral/Enteral Syringes with ENFit connector (1 mL to 6 mL), NeoConnect Oral/Enteral Syringes with ENFit connector (12 mL to 100 mL) and NeoConnect Low Dose Tip Oral/Enteral Syringes with ENFit connector (0.5 mL to 6mL), NeoMed NeoConnect Enteral Syringes with ENFit Connector and compatible NeoSecure Tip Caps
Neomed, Inc. has 13 FDA 510(k) cleared medical devices. Based in Swanee, US.
Historical record: 13 cleared submissions from 2007 to 2019. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Neomed, Inc. Filter by specialty or product code using the sidebar.