BURT

GUDID 00867504000413

BURT Rehabilitation System is indicated to aid in the rehabilitation and evaluation of upper extremities for patients suffering from neurological or musculoskeletal injuries or conditions. BURT is a robotic system with 3 actuators (DC motors) in the base, a relatively thin “arm” section composed of two links (“inner” and “outer”) connected via a rotating joint (driven by the 3rd actuator via cables), electronics to drive the system, firmware and software that control the system and provide therapeutic activities and games for the patient, and a stand that supports the system.

BARRETT TECHNOLOGY, LLC

Virtual-display rehabilitation system, powered-support
Primary Device ID00867504000413
NIH Device Record Keyea140002-d0d6-4dd3-a837-c8cd6caa4f7d
Commercial Distribution StatusIn Commercial Distribution
Brand NameBURT
Version Model NumberM1400
Company DUNS080108367
Company NameBARRETT TECHNOLOGY, LLC
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numbertrue
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone1 617 252 9000
Emailburtsupport@barrett.com
Phone1 617 252 9000
Emailburtsupport@barrett.com
Phone1 617 252 9000
Emailburtsupport@barrett.com
Phone1 617 252 9000
Emailburtsupport@barrett.com
Phone1 617 252 9000
Emailburtsupport@barrett.com
Phone1 617 252 9000
Emailburtsupport@barrett.com
Phone1 617 252 9000
Emailburtsupport@barrett.com
Phone1 617 252 9000
Emailburtsupport@barrett.com
Phone1 617 252 9000
Emailburtsupport@barrett.com
Phone1 617 252 9000
Emailburtsupport@barrett.com
Phone1 617 252 9000
Emailburtsupport@barrett.com
Phone1 617 252 9000
Emailburtsupport@barrett.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100867504000413 [Primary]

FDA Product Code

IKKSystem, Isokinetic Testing And Evaluation

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2018-12-17
Device Publish Date2018-11-15

On-Brand Devices [BURT]

00867504000413BURT Rehabilitation System is indicated to aid in the rehabilitation and evaluation of upper ext
00867504000406M1200

Trademark Results [BURT]

Mark Image

Registration | Serial
Company
Trademark
Application Date
BURT
BURT
87660617 5453566 Live/Registered
Drifter Tackle, Inc.
2017-10-26
BURT
BURT
87294205 5388150 Live/Registered
Barrett Technology, LLC
2017-01-09
BURT
BURT
85597236 4260757 Dead/Cancelled
Domtar Inc.
2012-04-13
BURT
BURT
76363750 not registered Dead/Abandoned
LGC Management, Inc.
2002-01-28
BURT
BURT
76308031 not registered Dead/Abandoned
LGC MANAGEMENT, INC.
2001-09-04
BURT
BURT
76059998 not registered Dead/Abandoned
Primal Combat Science, Inc.
2000-06-05
BURT
BURT
74545259 2021602 Dead/Cancelled
Zanella Ltd.
1994-06-29
BURT
BURT
73743076 1569251 Live/Registered
MATEER-BURT COMPANY
1988-07-29
BURT
BURT
73019691 1022730 Dead/Expired
GARCIA CORPORATION, THE
1974-04-24
BURT
BURT
72046597 0676522 Dead/Expired
F. N. BURT COMPANY, INC.
1958-02-26

© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.