Identity
- Trade Name
- AMA Optics Lens Holder FDA UDI
- Generic Name
- Trial lens FDA UDI
- Device Name
- An individual ophthalmic lens from a trial lens set. (lens holder) FDA UDI
- Model / Reference
- LH-01 FDA UDI
- Description
- An individual ophthalmic lens from a trial lens set. (lens holder) FDA UDI
Identifiers
- Catalog Number
- HOLDER01 FDA UDI
- Primary DI / UDI-DI
- G506HOLDER010 FDA UDI
- FDA Product Code
- HPC FDA UDI
- GMDN Term
- Trial lens FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 886.1405 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
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
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Trial lens
AMA Optics Lens Holder by AMA Optics, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Trial lens.
- AMA Optics Panoramic Pinhole — AMA Optics, Inc. · 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
- AMA Optics, Inc.
Sources (1)
- FDA UDI a317b258-e0b0-485f-bb04-4777d10c5550 34 fields · synced Jun 6, 2026