Product code HLF
- Device name
- Device, Measuring, Lens Radius, Ophthalmic
- Medical specialty
- Ophthalmic
- Device class
- 1
- Regulation number
- 886.1430
- Review panel
- OP
- Implant
- N
- Life sustaining/supporting
- N
- GMP exempt
- N
- Third party review
- N
- Summary malfunction reporting
- Eligible
- Source
- FDA openFDA device classification dataset
Related 510(k) Records#
Related GUDID Devices#
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|---|---|---|---|
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| 08175700107259 | Hoffer Optical Zone Marker | AURORA SURGICAL, LLC | 2024-07-11 |
| 08175700107402 | Bores Optical Zone Marker | AURORA SURGICAL, LLC | 2024-07-11 |
| 08175700107242 | Hoffer Optical Zone Marker | AURORA SURGICAL, LLC | 2024-07-11 |
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