Anacapa Technologies, Inc. is one of 16313 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Anacapa Technologies, Inc. - FDA 510(k) Cleared Devices
Recent clearances: ANASEPT ANTIMICROBIAL SKIN AND WOUND CLEANSERS, SILVER SHIELD ANTIMICROBIAL SKIN AND WOUND GEL, MODEL 3015-S
2
Total
2
Cleared
0
Denied
Anacapa Technologies, Inc. has 2 FDA 510(k) cleared medical devices. Based in San Dimas, US.
Historical record: 2 cleared submissions from 2006 to 2008. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Anacapa Technologies, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Anacapa Technologies, Inc.
2 devices