Identity
- Trade Name
- Kate Young FDA UDI
- Generic Name
- Spectacle frame FDA UDI
- Model / Reference
- K517 BLK 55 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00764724347789 FDA UDI
- FDA Product Code
- HQY FDA UDI
- GMDN Term
- Spectacle frame FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 886.5850 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
Yes
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
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Dimensions & Sizes
- Size
- Width — 55 Millimeter FDA UDI
Category: Spectacle frame
Kate Young by Tura Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- BBIG — BBig B.V. · Class I
- Fielmann — Fielmann Group AG · Class I
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
- Tura Inc.
Sources (1)
- FDA UDI a9268065-ec6e-463e-aded-eaec5a71d8dc 34 fields · synced May 31, 2026