iAssist

GUDID 00889024276185

Orthosoft Inc

Orthopaedic prosthesis implantation instrument, single-use
Primary Device ID00889024276185
NIH Device Record Keyddc7b9da-8a42-467e-9a33-18b5dd9bda04
Commercial Distribution StatusIn Commercial Distribution
Brand NameiAssist
Version Model Number20-8000-000-20
Company DUNS205670032
Company NameOrthosoft Inc
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 Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800)348-2759
Emailzimmer.consumerrelations@zimmer.com
Phone+1(800)348-2759
Emailzimmer.consumerrelations@zimmer.com
Phone+1(800)348-2759
Emailzimmer.consumerrelations@zimmer.com
Phone+1(800)348-2759
Emailzimmer.consumerrelations@zimmer.com
Phone+1(800)348-2759
Emailzimmer.consumerrelations@zimmer.com
Phone+1(800)348-2759
Emailzimmer.consumerrelations@zimmer.com
Phone+1(800)348-2759
Emailzimmer.consumerrelations@zimmer.com
Phone+1(800)348-2759
Emailzimmer.consumerrelations@zimmer.com
Phone+1(800)348-2759
Emailzimmer.consumerrelations@zimmer.com
Phone+1(800)348-2759
Emailzimmer.consumerrelations@zimmer.com
Phone+1(800)348-2759
Emailzimmer.consumerrelations@zimmer.com
Phone+1(800)348-2759
Emailzimmer.consumerrelations@zimmer.com
Phone+1(800)348-2759
Emailzimmer.consumerrelations@zimmer.com
Phone+1(800)348-2759
Emailzimmer.consumerrelations@zimmer.com
Phone+1(800)348-2759
Emailzimmer.consumerrelations@zimmer.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100889024276185 [Primary]

FDA Product Code

LXHORTHOPEDIC MANUAL SURGICAL INSTRUMENT

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2019-02-07
Device Publish Date2017-05-10

On-Brand Devices [iAssist]

0088902430549620-8011-065-00
0088902430548920-8011-064-00
0088902430547220-8011-063-00
0088902430525020-8011-002-00
0088902430524320-8011-001-00
0088902427618520-8000-000-20
00889024211636302.4001

Trademark Results [iAssist]

Mark Image

Registration | Serial
Company
Trademark
Application Date
IASSIST
IASSIST
97595075 not registered Live/Pending
Triangle Tube Phase III Co.
2022-09-16
IASSIST
IASSIST
90696907 not registered Live/Pending
Triangle Tube Phase III Co.
2021-05-07
IASSIST
IASSIST
86299323 not registered Dead/Abandoned
Stuart C. Irby Company
2014-06-03
IASSIST
IASSIST
85705606 4351660 Live/Registered
ZIMMER, INC.
2012-08-16
IASSIST
IASSIST
85125219 4061255 Live/Registered
AssistRX, Inc.
2010-09-08
IASSIST
IASSIST
79101806 4103905 Dead/Cancelled
SINTOKOGIO, LTD.
2011-07-19
IASSIST
IASSIST
76609005 3510344 Dead/Cancelled
Toshiba Medical Systems Corporation
2004-08-27

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.