HPXUnclassified
Lens, Contact (Polymethylmethacrylate)
Unknown
HPX is the FDA product code for Lens, Contact (Polymethylmethacrylate). As of , FDA records hold 74 510(k) clearances under this code, the most recent dated , and no recalls.
Classification record
- Product code
- HPX
- Device name
- Lens, Contact (Polymethylmethacrylate)
- Device class
- Unclassified
- Review panel
- Unknown
- Submission type
- 510(k)
- Implant
- No
- Life sustaining or supporting
- No
- GMP exempt
- No
- Third party review eligible
- No
- Ingested clearances
- 74
- Ingested recalls
- 0
Clearances, product code HPX
By decision yearShow the numbers
| Year | Clearances |
|---|---|
| 1976 | 4 |
| 1977 | 1 |
| 1978 | 2 |
| 1979 | 2 |
| 1980 | 4 |
| 1981 | 5 |
| 1982 | 18 |
| 1983 | 4 |
| 1984 | 3 |
| 1985 | 12 |
| 1986 | 12 |
| 1987 | 1 |
| 1988 | 1 |
| 1990 | 2 |
| 1991 | 1 |
| 1994 | 1 |
| 1996 | 1 |
Applicants with the most clearances
Product code HPX| Applicant | Clearances |
|---|---|
| Allergan | 8 |
| Maurry Biological Co. | 6 |
| Bausch & Lomb Incorporated | 5 |
| Optacryl, Inc. | 4 |
| Barnes-Hind, Inc. | 3 |
| Paco Pharmaceutical Services, Inc. | 3 |
| Applied Laboratories, Inc. | 2 |
| Blairex Laboratories, Inc. | 2 |
| CooperVision, Inc. | 2 |
| Optatint, Inc. | 2 |
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.
