NeoDevices, Inc. FTM5.0S
NeoDevices, Inc. FTM5.0S is a Class II device made by Neodevices Inc, listed in FDA GUDID since 24 Sep 2016 (UDI-DI 10816340020250), registry data as of 23 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number10816340020250 | Date24 Sep 2016 | StatusListed |
Official records
- AccessGUDID record 10816340020250
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- NeoDevices, Inc.
- Generic name
- Nasogastric feeding tube
- Model / reference
- FTM5.0S
- Primary DI / UDI-DI
- 10816340020250
- FDA product code
- KNT
- GMDN term
- Nasogastric feeding tube
- Device class
- Class II
- Regulation number
- 876.5980
- GUDID distribution status
- In Commercial Distribution
Similar devices
Other devices filed under FDA product code KNT (Tubes, Gastrointestinal (And Accessories)).
- NEEDLE CATHETER JEJUNOSTOMY KIT by BIOSEARCH MEDICAL PRODUCTS, INC.
- GASTRO-ENTEROSTOMY TUBE by Medical Innovations Corp.
- TubeClear System by ACTUATED MEDICAL, INC.
- CANTOR TUBE by Medovations, Inc.
- BLAKEMORE TUBE by Medovations, Inc.
- KANGAROO JEJUNAL FEEDING SYSTEM by Sherwood Medical Co.
- Kangaroo 386100 by Cardinal Health 200, LLC
- ENDOVIVE INITIAL PLACEMENT DIRECT PEJ KIT, ENDOVIVE STANDARD PROFILE BALLOON REPLACEMENT, MODELS 6520, 6521, 6220 by Boston Scientific
- FLEXIFLO NASOENTERIC FEEDING TUBE by Abbott Laboratories
- CORTRAK by Viasys Medsystems