Company ยท US
Litecure, LLC
FDA 510(k) clearances and medical device recalls filed under this name, 2007 to 2018. Name variants (Inc, Corp, punctuation) are merged.
7510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Feb 22, 2018 | K173067 | LightForce LTS Model 1000, 1500, 2500, and 4000 Litecure, LLC | GEX |
| Mar 29, 2013 | K123014 | LITECURE THERAPY SYSTEM MODEL LTS-1500 Litecure, LLC | PDZ |
| Dec 3, 2012 | K123031 | BWF-5 MEDICAL LASER SERIES Litecure, LLC | GEX |
| Jun 12, 2012 | K121487 | LITECURE THERAPY COMPACT Litecure, LLC | ILY |
| Jan 25, 2011 | K103511 | LITECURE THERAPY SYSTEM Litecure, LLC | ILY |
| May 12, 2010 | K093087 | BWF-5 MEDICAL LASER SERIES Litecure, LLC | GEX |
| Feb 28, 2007 | K070400 | LC THERAPY, MODEL LCT-1000 Litecure, LLC | ILY |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||