Identity
- Trade Name
- Liberty® FDA UDI
- Generic Name
- Air-conduction hearing aid, canal FDA UDI
- Device Name
- Lucid® FIO OTC FDA UDI
- Model / Reference
- 7287 FDA UDI
- Description
- Lucid® FIO OTC FDA UDI
Identifiers
- Catalog Number
- HLT-FIO FDA UDI
- Primary DI / UDI-DI
- 00810068830446 FDA UDI
- FDA Product Code
- QUG FDA UDI
- GMDN Term
- Air-conduction hearing aid, canal FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 874.3305 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
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
MR Unsafe FDA UDI
Category: Air-conduction hearing aid, canal
Liberty® by Hearing Lab Technology, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- KIND — Starkey Laboratories Inc. · Class II
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 II | Pending data |
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Manufacturer
- Manufacturer
- Hearing Lab Technology, Llc
Sources (1)
- FDA UDI 7f12d770-3c33-48f4-9e5b-add320c9755d 35 fields · synced May 30, 2026