LightStim Elipsa
by LED Intellectual Properties
510(k) K212771
LightStim Elipsa is a Class II device made by LED Intellectual Properties, cleared under FDA 510(k) K212771 on 26 Jan 2022, active as of 22 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK212771 | Date26 Jan 2022 | StatusActive |
Official records
- FDA 510(k) database K212771
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- OHS
- FDA applicant
- Led Intellectual Properties, LLC
- Device class
- Class II
- Regulation
- 21 CFR Part 878.4810
- Advisory committee
- General, Plastic Surgery
- FDA decision
- SESE Substantially Equivalent
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