The Anspach Effort, Inc. - FDA 510(k) Cleared Devices
60
Total
60
Cleared
0
Denied
The Anspach Effort, Inc. has 60 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Last cleared in 2022. Active since 1980.
Browse the FDA 510(k) cleared devices submitted by The Anspach Effort, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by The Anspach Effort, Inc.
60 devices
Cleared
May 19, 2022
Wireless Hand Control, EG1A (WIRELESS-HC), Receiver for Wireless Hand...
Neurology
91d
Cleared
Jul 19, 2019
Anspach Helix Dissection Tools
Neurology
211d
Cleared
Mar 27, 2018
OCM-G1 Attachment
Ear, Nose, Throat
77d
Cleared
Jan 10, 2014
ANSPACH EG1 HIGH SPEED SYSTEM, G1 ATTACHMENTS
Neurology
46d
Cleared
Dec 31, 2013
ANSPACH XMAX, EMAX2 AND EMAX2 PLUS SYSTEM WITH OTOLOGIC ATTACHMENT SYSTEM
Ear, Nose, Throat
259d
Cleared
Dec 16, 2011
ANSPACH DISSECTION TOOLS
Neurology
24d
Cleared
Dec 22, 2008
CRANIAL PERFORATOR
Neurology
103d
Cleared
Apr 30, 2008
EMAX 2 PLUS SYSTEM, MODEL EMAX 2 PLUS MOTOR, EMAX 2 CONSOLE>FIRMWARE...
Neurology
40d
Cleared
Jan 26, 2007
ANSPACH IMRI SAFE SURGICAL DRILL SYSTEM
Neurology
262d
Cleared
Jan 16, 2007
SURGICAL IRRIGATION SYSTEM, IRRIGATION TUBE
Orthopedic
35d
Cleared
Dec 05, 2005
ANSPACH KNOTLESS ANCHOR
Orthopedic
77d
Cleared
Apr 07, 2005
ANSPACH COUPLER
Neurology
27d
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