Medtec, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Medtec, Inc. - FDA 510(k) Cleared Devices
Recent clearances: TRUPOINT ARCH, NASION CUSHION, BITE CUP, TRUPOINT ARCH STORAGE PLATE, TRUPOINT ARCH BASE LOCK REPLACEMENT KIT, HEAD AND NECK IMMOBILIZATION SYSTEM, BODY IMMOBILIZATION SYSTEM, MRI PATIENT POSITIONING DEVICES
41
Total
41
Cleared
0
Denied
Medtec, Inc. has 41 FDA 510(k) cleared radiology devices. Based in Orange City, US.
Historical record: 41 cleared submissions from 1993 to 2014.
Browse the complete list of FDA 510(k) cleared radiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Medtec, Inc.
41 devices
Cleared
Mar 04, 2014
TRUPOINT ARCH, NASION CUSHION, BITE CUP, TRUPOINT ARCH STORAGE PLATE,...
Radiology
168d
Cleared
Jun 28, 2011
HEAD AND NECK IMMOBILIZATION SYSTEM, BODY IMMOBILIZATION SYSTEM
Radiology
47d
Cleared
May 14, 2010
MRI PATIENT POSITIONING DEVICES
Radiology
161d
Cleared
Mar 10, 1998
CARBON FIBER BREAST BOARD
Radiology
84d
Cleared
Mar 04, 1998
MATRIX MT-MX3
Radiology
78d
Cleared
Dec 05, 1997
CARBON FIBER CONFORMAL COUCH TOP
Radiology
58d
Cleared
Oct 01, 1996
INTRA-ORAL THERMOPLASTIC SHIELD
Radiology
88d
Cleared
May 24, 1996
GREEN TEC-2100
Radiology
192d
Cleared
Jan 05, 1996
ACRYSTEEL BLOCKING TRAY
Radiology
85d
Cleared
Dec 21, 1995
THERMOPLASTIC SHIELD
Radiology
87d
Cleared
Nov 14, 1995
MED-TEC HAND GRIP
Radiology
64d
Cleared
Oct 17, 1995
MEDTEC AUTOBLOT 2000
Microbiology
183d
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