Identity
- Trade Name
- PMMA FDA UDI
- Generic Name
- Hard corrective contact lens FDA UDI
- Device Name
- PMMA (polymethyl methacrylate) hard contact lens for daily wear FDA UDI
- Model / Reference
- 003 FDA UDI
- Description
- PMMA (polymethyl methacrylate) hard contact lens for daily wear FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00858174006003 FDA UDI
- 510(k) Number
- K895411 FDA UDI
- FDA Product Code
- HPX FDA UDI
- GMDN Term
- Hard corrective contact lens FDA UDI
Classification
- Device Class
- U 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
Yes
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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Hard corrective contact lens
Pmma by Lagado Corporation, The — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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 U | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Lagado Corporation, The
Sources (1)
- FDA UDI 73399476-58cb-47ab-a9a2-2ac48efda11e 34 fields · synced Jun 8, 2026