LDKUnclassified
Device, Sensing, Optical Contour
Unknown
LDK is the FDA product code for Device, Sensing, Optical Contour. As of , FDA records hold 8 510(k) clearances under this code, the most recent dated , and no recalls.
Classification record
- Product code
- LDK
- Device name
- Device, Sensing, Optical Contour
- Device class
- Unclassified
- Review panel
- Unknown
- Submission type
- FDA code 7
- Implant
- No
- Life sustaining or supporting
- No
- GMP exempt
- No
- Third party review eligible
- No
- Ingested clearances
- 8
- Ingested recalls
- 0
Clearances, product code LDK
By decision yearShow the numbers
| Year | Clearances |
|---|---|
| 1980 | 1 |
| 1985 | 2 |
| 1986 | 1 |
| 1994 | 1 |
| 2019 | 1 |
| 2023 | 2 |
Applicants with the most clearances
Product code LDK| Applicant | Clearances |
|---|---|
| Bio-Tek Instruments, Inc. | 1 |
| Cryos Technologies, Inc. | 1 |
| Far Orthopedics, Inc. | 1 |
| Momentum Health Inc. | 1 |
| Nsite, Inc. | 1 |
| Oxford Medilog, Inc. | 1 |
| Quantec Image Processing, Ltd. | 1 |
| Terran Biomedical Instruments | 1 |
Companies listing this code with FDA
Companies whose registered establishments list this codeFIRST ARTICLE / WEEKLY
What cleared, what was recalled, and what changed in the standards. One edition a week for the people who make medical devices.