Medtec, Inc.

FDA Regulatory Profile

Medtec, Inc. appears in FDA public data with 0 recalls, 41 510(k) clearances, 3 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on Mar 4, 2014.

Summary

Total Recalls
0
510(k) Clearances
41
Inspections
3
Compliance Actions
0

Known Names

Medtec, Med-Tec

Recent 510(k) Clearances

K-NumberDeviceDate
K132908TRUPOINT ARCH, NASION CUSHION, BITE CUP, TRUPOINT ARCH STORAGE PLATE, TRUPOINT ARCH BASE LOCK REPLACMar 4, 2014
K111340HEAD AND NECK IMMOBILIZATION SYSTEM, BODY IMMOBILIZATION SYSTEMJun 28, 2011
K093738MRI PATIENT POSITIONING DEVICESMay 14, 2010
K974703CARBON FIBER BREAST BOARDMar 10, 1998
K974700MATRIX MT-MX3Mar 4, 1998
K973842CARBON FIBER CONFORMAL COUCH TOPDec 5, 1997
K962622INTRA-ORAL THERMOPLASTIC SHIELDOct 1, 1996
K955236GREEN TEC-2100May 24, 1996
K954705ACRYSTEEL BLOCKING TRAYJan 5, 1996
K954456THERMOPLASTIC SHIELDDec 21, 1995
K954225MED-TEC HAND GRIPNov 14, 1995
K951753MEDTEC AUTOBLOT 2000Oct 17, 1995
K952729PAINTED WEDGE & ROD BREAST BOARDSep 15, 1995
K950293TEC-2110 GREEN LASER MODEL MT-HNGAug 18, 1995
K952189MED-TEC REDISETAug 9, 1995
K950075MED-TEC TRAY ADAPTERJul 13, 1995
K951947MED-TEC RADIO THERAPY TREATMENT CHAIRJul 12, 1995
K951679MED-TEC TESTICULAR SEPARATORJul 12, 1995
K951808MED-TEC REDI-FOAMJul 6, 1995
K951717MED-TEC KNEE CRUTCHJun 28, 1995