Perfectio LED infrared device
K152332 is the FDA 510(k) clearance record for Perfectio LED infrared device, a class II device, cleared for Omm Imports Inc Dba Zero Gravity on under FDA product code OHS (Light Based Over The Counter Wrinkle Reduction). FDA's definition for product code OHS reads: "Use of light based treatment to reduce wrinkles on the body in general or specific anatomical locations depending on the information provided". FDA records list 3 510(k) clearances for OMM IMPORTS, INC. D/B/A ZERO GRAVITY, from to . As of , FDA records show no recalls naming K152332.
Clearance record
- Decision date
- Received
- (191 days to decision)
- Product code
- OHS Light Based Over The Counter Wrinkle Reduction
- Regulation
- 21 CFR 878.4810
- Device class
- Class II
- Review panel
- General, Plastic Surgery
- Applicant
- Omm Imports Inc Dba Zero Gravity 1945 S Ocean Dr. Apt.509 Hallandle Beach Blvd., Hallandle FL
- 510(k) summary
- Summary PDF
- Third party review
- No
Clearances, product code OHS
Trailing 12 monthsShow the numbers
| Month | Clearances |
|---|---|
| November 2025 | 3 |
| December 2025 | 8 |
| January 2026 | 3 |
| February 2026 | 2 |
| March 2026 | 4 |
| April 2026 | 1 |
| May 2026 | 1 |
| June 2026 | 4 |
| July 2026 | 4 |
| August 2026 | 5 |
| September 2026 | 0 |
| October 2026 | 0 |
FIRST ARTICLE / WEEKLY
What cleared, what was recalled, and what changed in the standards. One edition a week for the people who make medical devices.
