Continuum® Trilogy® Allofit® Longevity®

GUDID 00889024149076

Zimmer, Inc.

Non-constrained polyethylene acetabular liner
Primary Device ID00889024149076
NIH Device Record Keyd4ae0721-8767-42ca-bf7c-70e9f8df0804
Commercial Distribution StatusIn Commercial Distribution
Brand NameContinuum® Trilogy® Allofit® Longevity®
Version Model Number00-8751-008-28
Company DUNS056038268
Company NameZimmer, Inc.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
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@zimmerbiomet.com
Phone+1(800)348-2759
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(800)348-2759
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(800)348-2759
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(800)348-2759
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(800)348-2759
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(800)348-2759
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(800)348-2759
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(800)348-2759
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(800)348-2759
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(800)348-2759
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(800)348-2759
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(800)348-2759
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(800)348-2759
Emailzimmer.consumerrelations@zimmerbiomet.com

Device Dimensions

Lumen/Inner Diameter28 Millimeter
Device Size Text, specify0
Lumen/Inner Diameter28 Millimeter
Device Size Text, specify0
Lumen/Inner Diameter28 Millimeter
Device Size Text, specify0
Lumen/Inner Diameter28 Millimeter
Device Size Text, specify0
Lumen/Inner Diameter28 Millimeter
Device Size Text, specify0
Lumen/Inner Diameter28 Millimeter
Device Size Text, specify0
Lumen/Inner Diameter28 Millimeter
Device Size Text, specify0
Lumen/Inner Diameter28 Millimeter
Device Size Text, specify0
Lumen/Inner Diameter28 Millimeter
Device Size Text, specify0
Lumen/Inner Diameter28 Millimeter
Device Size Text, specify0
Lumen/Inner Diameter28 Millimeter
Device Size Text, specify0
Lumen/Inner Diameter28 Millimeter
Device Size Text, specify0
Lumen/Inner Diameter28 Millimeter
Device Size Text, specify0
Lumen/Inner Diameter28 Millimeter
Device Size Text, specify0
Lumen/Inner Diameter28 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS100889024149076 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

LZOProsthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2015-09-17

On-Brand Devices [Continuum® Trilogy® Allofit® Longevity®]

0088902415237300-8790-014-36
0088902415236600-8790-014-32
0088902415235900-8790-014-28
0088902415228100-8790-009-36
0088902415227400-8790-009-32
0088902415226700-8790-009-28
0088902415225000-8790-007-36
0088902415224300-8790-007-32
0088902415223600-8790-007-28
0088902415207600-8758-023-36
0088902415206900-8758-023-32
0088902415205200-8758-022-36
0088902415204500-8758-022-32
0088902415203800-8758-021-36
0088902415202100-8758-021-32
0088902415201400-8758-020-36
0088902415200700-8758-020-32
0088902415199400-8758-019-36
0088902415198700-8758-019-32
0088902415197000-8758-018-36
0088902415196300-8758-018-32
0088902415195600-8758-017-36
0088902415194900-8758-017-32
0088902415193200-8758-016-36
0088902415192500-8758-016-32
0088902415191800-8758-015-36
0088902415190100-8758-015-32
0088902415189500-8758-014-36
0088902415188800-8758-014-32
0088902415187100-8758-013-32
0088902415186400-8758-013-28
0088902415185700-8758-012-32
0088902415184000-8758-012-28
0088902415183300-8758-011-28
0088902415182600-8758-010-28
0088902415181900-8758-009-28
0088902415006500-8752-023-36
0088902415005800-8752-023-32
0088902415004100-8752-022-36
0088902415003400-8752-022-32
0088902415002700-8752-021-36
0088902415001000-8752-021-32
0088902415000300-8752-020-36
0088902414999100-8752-020-32
0088902414998400-8752-019-36
0088902414997700-8752-019-32
0088902414961800-8752-005-22
0088902415117800-8755-023-36
0088902415116100-8755-023-32
0088902415115400-8755-022-36

Trademark Results [Continuum]

Mark Image

Registration | Serial
Company
Trademark
Application Date
CONTINUUM
CONTINUUM
98852004 not registered Live/Pending
Commonwealth Equity Services, LLC
2024-11-13
CONTINUUM
CONTINUUM
98851650 not registered Live/Pending
Commonwealth Equity Services, LLC
2024-11-13
CONTINUUM
CONTINUUM
98404041 not registered Live/Pending
CONTINUUM LLC
2024-02-13
CONTINUUM
CONTINUUM
98404038 not registered Live/Pending
CONTINUUM LLC
2024-02-13
CONTINUUM
CONTINUUM
98384427 not registered Live/Pending
Starkey Laboratories, Inc.
2024-01-31
CONTINUUM
CONTINUUM
98298988 not registered Live/Pending
666 Performance, LLC
2023-12-05
CONTINUUM
CONTINUUM
98186670 not registered Live/Pending
Peters, Michael D.
2023-09-19
CONTINUUM
CONTINUUM
98055147 not registered Live/Pending
VentureSonic, LLC
2023-06-22
CONTINUUM
CONTINUUM
97897264 not registered Live/Pending
Continuum Global Solutions, LLC
2023-04-19
CONTINUUM
CONTINUUM
97748610 not registered Live/Pending
PeggyBack LLC
2023-01-10
CONTINUUM
CONTINUUM
97739741 not registered Live/Pending
Mestek, Inc.
2023-01-03
CONTINUUM
CONTINUUM
97677972 not registered Live/Pending
B & W Custom Truck Beds, Inc.
2022-11-15

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