Product code
NUU: Lens, contact, orthokeratology, overnight
FDA product code · Class III · Ophthalmic
Key facts
| Product code | NUU |
|---|---|
| Device | Lens, contact, orthokeratology, overnight |
| Device class | Class III |
| Regulation number | 886.5916 |
| Review panel | Ophthalmic |
| Medical specialty | Ophthalmic |
| Submission type | PMA |
| GMP exempt | No |
| Implanted device | No |
| Life-sustaining or life-supporting | No |
| Definition | Temporary reduction of myopia or refractive error. |
At a glance
- None 510(k) clearances
- None De Novo grants
- 1–9 PMA approvals
- None HDE approvals
- 10–99 UDI devices (GUDID)
- 10–99 MAUDE adverse event reports
- 1–9 Recalled products (Z-numbers)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device product codes
FDA product codes classify medical devices by type and intended use; each code maps to a device class, a classification regulation and a review panel.
Source: U.S. Food and Drug Administration (FDA), Product Classification database