Safety Syringes, Inc. is one of 10038 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Safety Syringes, Inc. - FDA 510(k) Cleared Devices
Recent clearances: ULTRASAFE INJECTION SYSTEM MODEL C200 INJECTOR WITH NEEDLE GUARD, ULTRASAFE MODEL T200 INJECTOR, ULTRASAFE INJECTION SYSTEM NEEDLE GUARD, MODELS B50,B100L,B150,B225, AND B300
10
Total
10
Cleared
0
Denied
Safety Syringes, Inc. has 10 FDA 510(k) cleared general hospital devices. Based in Arcadia, US.
Historical record: 10 cleared submissions from 1995 to 2013.
Browse the complete list of FDA 510(k) cleared general hospital devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Safety Syringes, Inc.
10 devices
Cleared
Mar 26, 2013
ULTRASAFE PLUS PASSIVE NEEDLE GUARD
General Hospital
110d
Cleared
Sep 20, 2012
ULTRASAFE PASSIVE NEEDLE GUARD
General Hospital
29d
Cleared
Apr 28, 2006
MODIFICATION TO: TAMPER EVIDENT ULTRASAFE PASSIVE DELIVERY SYSTEM, ULTRASAFE...
General Hospital
39d
Cleared
Oct 15, 2004
TAMPER EVIDENT ULTRASAFE PASSIVE DELIVERY SYSTEM
General Hospital
15d
Cleared
Dec 13, 2001
ULTRASAFE DENTAL INJECTION SYSTEM
General Hospital
28d
Cleared
May 29, 2001
ULTRASAFE PASSIVE X-SERIES, NEEDLE GUARD SYRINGE, PISTON (ACCESSORY)
General Hospital
25d
Cleared
Feb 26, 1998
ULTRASAFE INJECTION SYSTEM MODEL C200 INJECTOR WITH NEEDLE GUARD
General Hospital
206d
Cleared
Feb 26, 1998
ULTRASAFE MODEL T200 INJECTOR
General Hospital
204d
Cleared
Oct 30, 1997
ULTRASAFE INJECTION SYSTEM NEEDLE GUARD, MODELS B50,B100L,B150,B225, AND B300
General Hospital
87d
Cleared
Jan 26, 1995
ULTRASAFE ASPIRATING SYRINGE
General Hospital
136d