ClearanceBrief
Company ยท US

Restorative Therapies, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 2005 to 2017. Name variants (Inc, Corp, punctuation) are merged.

10510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
GZIStimulator, Neuromuscular, External Functional9
IPFStimulator, Muscle, Powered1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Jul 11, 2017K162470RT300 FES cycle ergometer
Restorative Therapies, Inc.
GZI
Dec 16, 2016K160614Xcite Clinical Station
Restorative Therapies, Inc.
IPF
Apr 5, 2011K103370RT200
Restorative Therapies, Inc.
GZI
Apr 4, 2011K103366RT600
Restorative Therapies, Inc.
GZI
Aug 5, 2009K090750RT300-SL, MODEL FA100052; RT300-SLSA, MODEL FA104581
Restorative Therapies, Inc.
GZI
Nov 21, 2007K072398RT300-S AND RT300-SP FES CYCLE ERGOMETER
Restorative Therapies, Inc.
GZI
Sep 10, 2007K071486RT300-S, RT300-SP (PEDIATRIC VERSION), MODEL FA100052, FA100053
Restorative Therapies, Inc.
GZI
Jul 5, 2007K071113RT300-S, MODEL FA100052, RT300-SP (PEDIATRIC VERSION), MODEL FA100053
Restorative Therapies, Inc.
GZI
Mar 10, 2006K060032RT300-S, MODEL FA100052; RT300-SP, MODEL FA100053
Restorative Therapies, Inc.
GZI
Jun 27, 2005K050036FES CYCLE ERGOMETER, MODEL RT300-S
Restorative Therapies, Inc.
GZI

Latest recalls

DateFirm and productCodeLinked 510(k)
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