Neodevices Inc
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Neodevices Inc is a medical device manufacturer, with 143 devices listed in FDA GUDID (FDA Class II) as of 14 Nov 2026.
- Devices
- 143
Registry facts
- Registries
- FDA GUDID 143
- Device classes
- FDA Class II 143
- Identifiers
- DUNS 189670230
What Neodevices Inc makes
NeoDevices Inc. manufactures single-use and reusable medical devices for critical clinical applications, including nasogastric feeding tubes, intravenous tubing extensions, and ENFit-compatible oral/enteral syringes. Their portfolio also covers sterile connectors for catheters and gastrostomy tubes, blood transfusion sets, and disposable spinal needles, alongside reusable utility forceps for procedural use.
All listed devices fall under Class II regulatory classification in the U.S., with each product authorised via the FDA’s Unique Device Identification (UDI) system. The company’s devices are registered under the FDA’s UDI database, reflecting compliance with U.S. medical device regulations.
Catalogue
Search and filter all 143 devicesShowing 1-50 of 143
Company details
- DUNS number
- 189670230
- info@neodevices.com
- Phone
- 866-636-6285
Frequently asked questions
How many devices does NEODEVICES INC have in the registry?
The registry currently lists 143 devices for NEODEVICES INC. Devices recorded under merged duplicate company entries are counted once.
Which registries list NEODEVICES INC's devices?
Among its 50 most recently registered devices, NEODEVICES INC has devices listed in FDA GUDID (50 devices).
What risk classes do NEODEVICES INC's devices fall under?
Among its 50 most recently registered devices, the classes recorded for NEODEVICES INC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from NEODEVICES INC in the registry?
The most recently registered devices listed for NEODEVICES INC include ND60EL-HF, EL-SPIKE-M, EL-SPIKE-F and EL-S55-HF.