HMPClass I
Pad, Eye
21 CFR 878.4440 / General, Plastic Surgery
HMP is the FDA product code for Pad, Eye, a class I device type, regulated under 21 CFR 878.4440. As of , FDA records hold 17 510(k) clearances under this code, the most recent dated , and 4 recalls.
Classification record
- Product code
- HMP
- Device name
- Pad, Eye
- Regulation
- 21 CFR 878.4440
- Device class
- Class I
- Review panel
- General, Plastic Surgery
- Submission type
- 510(k) exempt
- Implant
- No
- Life sustaining or supporting
- No
- GMP exempt
- No
- Third party review eligible
- No
- Ingested clearances
- 17
- Ingested recalls
- 4
Clearances, product code HMP
By decision yearShow the numbers
| Year | Clearances |
|---|---|
| 1978 | 1 |
| 1980 | 3 |
| 1981 | 1 |
| 1984 | 1 |
| 1985 | 3 |
| 1986 | 2 |
| 1987 | 1 |
| 1988 | 2 |
| 1990 | 1 |
| 1992 | 1 |
| 1994 | 1 |
Applicants with the most clearances
Product code HMP| Applicant | Clearances |
|---|---|
| Keeler Instruments, Inc. | 2 |
| Certified Safety Mfg Inc | 1 |
| Conphar, Inc. | 1 |
| Consolidated Industries of Greater Syracuse, Inc. | 1 |
| DeRoyal Industries, Inc. | 1 |
| M.S.G. Health Systems, Inc. | 1 |
| Medi-Spec | 1 |
| Nice-Pak Products, LLC | 1 |
| Pantheon Products, Inc. | 1 |
| Pollak (Intl.).ltd | 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.