Entific Medical Systems, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Entific Medical Systems, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Entific Medical Systems, Inc. has 5 FDA 510(k) cleared medical devices. Based in Findley, US.
Historical record: 5 cleared submissions from 1999 to 2004. Primary specialty: Ear, Nose, Throat.
Browse the FDA 510(k) cleared devices submitted by Entific Medical Systems, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Entific Medical Systems, Inc.
5 devices
Cleared
Aug 26, 2004
BAHA DIVINO
Ear, Nose, Throat
30d
Cleared
Aug 30, 2002
BRANENMARK BONE-ANCHORED-HEARING AID (BAHA)
Ear, Nose, Throat
87d
Cleared
Jul 23, 2001
BILATERAL FITTING OF THE BRANEMARK BONE-ANCHORED HEARING AID (BAHA) SYSTEM.
Ear, Nose, Throat
74d
Cleared
Oct 17, 2000
HEADBAND FOR BAHA
Ear, Nose, Throat
29d
Cleared
Nov 24, 1999
BRANEMARK BONE-ANCHORED HEARING AID (BAHA) CORDELLE II
Ear, Nose, Throat
90d