Ergoline Vitality Total Light 3, Planet Fitness 50/4 TLT by Ergoline, Planet Fitness 42/3 TLT by Ergoline, Ergoline Vitality Hybrid Light 3, Ergoline Vitality Hybrid Light, Planet Fitness 50/4 HLT by Ergoline, Planet Fitness 46/3 HLT by Ergoline, Ergoline Vitality Pure Light 3, Ergoline Vitality Pure Light, Planet Fitness 50/4 PLT III by Ergoline, Planet Fitness 50/4 PLT by Ergoline, Planet Fitness 46/3 PLT by Ergoline, Planet Fitness 42/3 PLT by Ergoline
K220500 is the FDA 510(k) clearance record for Ergoline Vitality Total Light 3, Planet Fitness 50/4 TLT by Ergoline, Planet Fitness 42/3 TLT by Ergoline, Ergoline Vitality Hybrid Light 3, Ergoline Vitality Hybrid Light, Planet Fitness 50/4 HLT by Ergoline, Planet Fitness 46/3 HLT by Ergoline, Ergoline Vitality Pure Light 3, Ergoline Vitality Pure Light, Planet Fitness 50/4 PLT III by Ergoline, Planet Fitness 50/4 PLT by Ergoline, Planet Fitness 46/3 PLT by Ergoline, Planet Fitness 42/3 PLT by Ergoline, a class II device, cleared for Jk-Holding GmbH on under FDA product code LEJ (Booth, Sun Tan). FDA records list 6 510(k) clearances for Jk-Holding GmbH, from to . As of , FDA records show no recalls naming K220500.
Clearance record
- Decision date
- Received
- (129 days to decision)
- Product code
- LEJ Booth, Sun Tan
- Regulation
- 21 CFR 878.4635
- Device class
- Class II
- Review panel
- General, Plastic Surgery
- Applicant
- Jk-Holding GmbH Koehlershohner Strasse 60, Windhagen, DE
- 510(k) summary
- Summary PDF
- Third party review
- No
Clearances, product code LEJ
Trailing 12 monthsFDA records hold no clearances under product code LEJ in the trailing twelve months.
Show the numbers
| Month | Clearances |
|---|---|
| November 2025 | 0 |
| December 2025 | 0 |
| January 2026 | 0 |
| February 2026 | 0 |
| March 2026 | 0 |
| April 2026 | 0 |
| May 2026 | 0 |
| June 2026 | 0 |
| July 2026 | 0 |
| August 2026 | 0 |
| September 2026 | 0 |
| October 2026 | 0 |
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