Litecure, LLC
Litecure, LLC appears in FDA public data with 0 recalls, 7 510(k) clearances, 1 FDA inspection, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on February 22, 2018.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 7
- Inspections
- 1
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K173067 | LightForce LTS Model 1000, 1500, 2500, and 4000 | February 22, 2018 |
| K123014 | LITECURE THERAPY SYSTEM MODEL LTS-1500 | March 29, 2013 |
| K123031 | BWF-5 MEDICAL LASER SERIES | December 3, 2012 |
| K121487 | LITECURE THERAPY COMPACT | June 12, 2012 |
| K103511 | LITECURE THERAPY SYSTEM | January 25, 2011 |
| K093087 | BWF-5 MEDICAL LASER SERIES | May 12, 2010 |
| K070400 | LC THERAPY, MODEL LCT-1000 | February 28, 2007 |