NeoDevices, Inc. LN2210
NeoDevices, Inc. LN2210 is a Class II device made by Neodevices Inc, listed in FDA GUDID since 24 Sep 2016 (UDI-DI 10816340021097), 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 | Number10816340021097 | Date24 Sep 2016 | StatusListed |
Official records
- AccessGUDID record 10816340021097
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- NeoDevices, Inc.
- Generic name
- Spinal needle, single-use
- Model / reference
- LN2210
- Primary DI / UDI-DI
- 10816340021097
- FDA product code
- FMI
- GMDN term
- Spinal needle, single-use
- Device class
- Class II
- Regulation number
- 880.5570
- GUDID distribution status
- In Commercial Distribution
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