Endocare, Inc. is one of 15055 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Endocare, Inc. - FDA 510(k) Cleared Devices
Recent clearances: CRYOCARE CS SURGICAL SYSTEM, CRYOCARE CN2 SYSTEM, CRYOCARE CS SURGICAL SYSTEM
22
Total
22
Cleared
0
Denied
Endocare, Inc. has 22 FDA 510(k) cleared medical devices. Based in Irvine, US.
Historical record: 22 cleared submissions from 1996 to 2010. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Endocare, Inc. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Tuv America, Inc., Regulatory Technology Services, LLC and Underwriters Laboratories, Inc..
FDA 510(k) Regulatory Record - Endocare, Inc.
22 devices
Cleared
Jun 14, 2010
CRYOCARE CS SURGICAL SYSTEM
General & Plastic Surgery
33d
Cleared
Aug 28, 2006
CRYOCARE CN2 SYSTEM
General & Plastic Surgery
28d
Cleared
Feb 28, 2006
CRYOCARE CS SURGICAL SYSTEM
General & Plastic Surgery
26d
Cleared
Feb 25, 2005
MODIFICATION TO CRYOCARE CS SURGICAL SYSTEM
Radiology
14d
Cleared
Aug 12, 2003
CRYOCARE CS SURGICAL SYSTEM
Radiology
14d
Cleared
Dec 05, 2002
CRYOCARE SURGICAL SYSTEM, MODEL CRYO 20
General & Plastic Surgery
27d
Cleared
Jun 06, 2002
MODIFIED CARDIAC CRYOSURGICAL SYSTEM, MODELS 6TCS1 & 6TCSE
Cardiovascular
69d
Cleared
Feb 05, 2002
ERECAID CLASSIC SYSTEM
Gastroenterology & Urology
26d
Cleared
Jan 25, 2002
CRYOCARE SURGICAL SYSTEM
General & Plastic Surgery
291d
Cleared
Oct 11, 2001
CRYOCARE SURGICAL SYSTEM
General & Plastic Surgery
304d
Cleared
Jun 15, 2001
CRYOCARE CARDIAC SURGICAL SYSTEM
Cardiovascular
71d
Cleared
May 03, 2001
SANARUS CORE TISSUE BIOPSY SYSTEM
Gastroenterology & Urology
168d