Axya Medical, Inc. - FDA 510(k) Cleared Devices
19
Total
19
Cleared
0
Denied
Axya Medical, Inc. has 19 FDA 510(k) cleared medical devices. Based in Beverly, US.
Historical record: 19 cleared submissions from 1998 to 2007. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Axya Medical, Inc. Filter by specialty or product code using the sidebar.
19 devices
Cleared
Oct 11, 2007
AXYA, MODEL 3000 AXYZLOOP TITANIUM BONE ANCHOR
Orthopedic
204d
Cleared
Jul 11, 2007
AXYA SUTURE WELDING SYSTEM AND KIT
General & Plastic Surgery
166d
Cleared
Dec 04, 2006
TUFFLEX POLYESTER SUTURE
General & Plastic Surgery
45d
Cleared
Sep 01, 2006
AXYAFLEX POLYESTER SUTURE
General & Plastic Surgery
221d
Cleared
Jul 05, 2006
AXYALOOP NONABSORBABLE BONE ANCHOR
Orthopedic
89d
Cleared
Oct 07, 2005
AXYA MODEL 6500 AXYALOOP SELF-TAPPING BONE ANCHOR
Orthopedic
25d
Cleared
Aug 05, 2005
MODEL 3000 AXYALOOP BIO-ABSORBABLE BONE ANCHOR
Orthopedic
14d
Cleared
Jun 09, 2005
AXYA, MODEL 6500 AXYALOOP BIO-ABSORBABLE BONE ANCHOR
Orthopedic
24d
Cleared
Oct 05, 2004
AXYA MEDICAL, INC. MODEL 5000 AXYALOOP BIO-ABSORBABLE BONE ANCHOR
Orthopedic
105d
Cleared
Oct 04, 2002
AXYA MODEL 3000 AXYALOOP TITANIUM BONE ANCHOR SYSTEM
Orthopedic
88d
Cleared
Sep 10, 2002
AXYA MEDICAL, INC, MODEL 100 SONIC SCALPEL ULTRASONIC SURGICAL SYSTEM
General & Plastic Surgery
90d
Cleared
Aug 31, 2001
MODEL 2000 AXYALOOP SELF-TAPPING BONE ANCHOR, MODEL 2000
Orthopedic
73d