Identity
- Trade Name
- NeoSpoon™ FDA UDI
- Generic Name
- Medicine spoon, single-use FDA UDI
- Device Name
- NeoSpoon is intended for use as a measuring device. FDA UDI
- Model / Reference
- 1/8 tsp and 1/2 tsp FDA UDI
- Description
- NeoSpoon is intended for use as a measuring device. FDA UDI
Identifiers
- Catalog Number
- N761 FDA UDI
- Primary DI / UDI-DI
- 10812594012157 FDA UDI
- FDA Product Code
- KYW FDA UDI
- GMDN Term
- Medicine spoon, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 880.6430 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Medicine spoon, single-use
NeoSpoon™ by Neotech Products LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Neotech Products LLC
Sources (1)
- FDA UDI 129e5f93-e472-4f8a-90de-df225d953d76 34 fields · synced Jun 8, 2026