Aesculap is one of 20751 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Aesculap - FDA 510(k) Cleared Devices
Recent clearances: AESCULAP STERILCONTAINER S, S4 SPINAL SYSTEM, AESCULAP STERILCONTAINER SYSTEM
10
Total
10
Cleared
0
Denied
Aesculap has 10 FDA 510(k) cleared medical devices. Based in Center Valley, US.
Historical record: 10 cleared submissions from 2003 to 2010.
Browse the FDA 510(k) cleared devices submitted by Aesculap Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Tuv America, Inc. and Aesculap AG.
FDA 510(k) Regulatory Record - Aesculap
10 devices
Cleared
May 11, 2010
AESCULAP STERILCONTAINER S
General Hospital
167d
Cleared
Mar 02, 2007
S4 SPINAL SYSTEM
Orthopedic
224d
Cleared
Nov 17, 2006
AESCULAP STERILCONTAINER SYSTEM
General Hospital
81d
Cleared
Jul 11, 2006
MINOP DISPOSABLE INTRODUCER 10F, MODEL ME010
Neurology
78d
Cleared
Dec 08, 2004
BICONTACT HIP SYSTEM WITH U-CAP
Orthopedic
30d
Cleared
Dec 06, 2004
AESCULAP STERRAD 100S COMPATABLE STERILCONTAINER
General Hospital
248d
Cleared
Aug 25, 2004
BICONTACT HIP STEM AND FEMORAL HEAD
Orthopedic
210d
Cleared
Jun 17, 2004
CRANIOFIX AND CRANIOFIX2 TITANIUM CLAMP SYSTEM
Neurology
76d
Cleared
Jul 17, 2003
MONOPLUS POLY-P-DIOXANONE MONOFILAMENT ABSORBABLE SURGICAL SUTURE
General & Plastic Surgery
91d
Cleared
May 09, 2003
AESCULAP NEURO PATTIES, NEUROSORB 4, 6, AND 75 (GREEN & WHITE)
Neurology
39d