Zap Lasers, LLC is one of 21628 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Zap Lasers, LLC - FDA 510(k) Cleared Devices
Recent clearances: SOFTLASE PRO, ORTHOLASE AND HYGIENELASE, STYLA MICROLASER AND STYLAORTHO, SOFTLASE G2-SURGICAL DIODE LASER SYSTEM
3
Total
3
Cleared
0
Denied
Zap Lasers, LLC has 3 FDA 510(k) cleared medical devices. Based in Pleasant Hill, US.
Historical record: 3 cleared submissions from 2002 to 2009. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Zap Lasers, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Underwriters Laboratories, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Zap Lasers, LLC
3 devices