BodyForm™ 19-11-0055

GUDID 10889981057909

Thoracic 55mm Bone Screw

SEASPINE ORTHOPEDICS CORPORATION

Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable Spinal fixation plate, non-bioabsorbable
Primary Device ID10889981057909
NIH Device Record Key358ab83b-5e5a-4b3e-9b20-abac385ffecb
Commercial Distribution StatusIn Commercial Distribution
Brand NameBodyForm™
Version Model Number19-11-0055
Catalog Number19-11-0055
Company DUNS079840876
Company NameSEASPINE ORTHOPEDICS CORPORATION
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 Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(760)727-8399
Emailcustsvcspine@seaspine.com
Phone+1(760)727-8399
Emailcustsvcspine@seaspine.com
Phone+1(760)727-8399
Emailcustsvcspine@seaspine.com
Phone+1(760)727-8399
Emailcustsvcspine@seaspine.com
Phone+1(760)727-8399
Emailcustsvcspine@seaspine.com
Phone+1(760)727-8399
Emailcustsvcspine@seaspine.com
Phone+1(760)727-8399
Emailcustsvcspine@seaspine.com
Phone+1(760)727-8399
Emailcustsvcspine@seaspine.com
Phone+1(760)727-8399
Emailcustsvcspine@seaspine.com
Phone+1(760)727-8399
Emailcustsvcspine@seaspine.com
Phone+1(760)727-8399
Emailcustsvcspine@seaspine.com
Phone+1(760)727-8399
Emailcustsvcspine@seaspine.com
Phone+1(760)727-8399
Emailcustsvcspine@seaspine.com
Phone+1(760)727-8399
Emailcustsvcspine@seaspine.com
Phone+1(760)727-8399
Emailcustsvcspine@seaspine.com

Device Dimensions

Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS110889981057909 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

KWQAPPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[10889981057909]

Moist Heat or Steam Sterilization


[10889981057909]

Moist Heat or Steam Sterilization


[10889981057909]

Moist Heat or Steam Sterilization


[10889981057909]

Moist Heat or Steam Sterilization


[10889981057909]

Moist Heat or Steam Sterilization


[10889981057909]

Moist Heat or Steam Sterilization


[10889981057909]

Moist Heat or Steam Sterilization


[10889981057909]

Moist Heat or Steam Sterilization


[10889981057909]

Moist Heat or Steam Sterilization


[10889981057909]

Moist Heat or Steam Sterilization


[10889981057909]

Moist Heat or Steam Sterilization


[10889981057909]

Moist Heat or Steam Sterilization


[10889981057909]

Moist Heat or Steam Sterilization


[10889981057909]

Moist Heat or Steam Sterilization


[10889981057909]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2015-09-24

On-Brand Devices [BodyForm™]

10889981062194BodyForm Thoraco-Lumbar Fixation System
10889981057923Thoracic Set Screw
10889981057916Thoracic 60mm Bone Screw
10889981057909Thoracic 55mm Bone Screw
10889981057893Thoracic 50mm Bone Screw
10889981057886Thoracic 45mm Bone Screw
10889981057879Thoracic 40mm Bone Screw
10889981057862Thoracic 35mm Bone Screw
10889981057855Thoracic 30mm Bone Screw
10889981057848Thoracic 25mm Bone Screw
10889981057831Thoracic 20mm Bone Screw
10889981057824Thoracic 99mm Plate
10889981057817Thoracic 95mm Plate
10889981057800Thoracic 91mm Plate
10889981057794Thoracic 87mm Plate
10889981057787Thoracic 83mm Plate
10889981057770Thoracic 79mm Plate
10889981057763Thoracic 76mm Plate
10889981057756Thoracic 73mm Plate
10889981057749Thoracic 70mm Plate
10889981057732Thoracic 67mm Plate
10889981057725Thoracic 64mm Plate
10889981057718Thoracic 62mm Plate
10889981057701Thoracic 60mm Plate
10889981057695Thoracic 44mm Plate
10889981057688Thoracic 43mm Plate
10889981057671Thoracic 42mm Plate
10889981057664Thoracic 41mm Plate
10889981057657Thoracic 40mm Plate

Trademark Results [BodyForm]

Mark Image

Registration | Serial
Company
Trademark
Application Date
BODYFORM
BODYFORM
88889700 not registered Live/Pending
Precare Corp.
2020-04-27
BODYFORM
BODYFORM
86598276 4858875 Live/Registered
Brookstone Purchasing, Inc.
2015-04-15
BODYFORM
BODYFORM
79330961 not registered Live/Pending
Applications Mobiles Overview Inc.
2021-10-22
BODYFORM
BODYFORM
78899887 not registered Dead/Abandoned
LIGHTHOUSE TRADEMARKS, S.L.
2006-06-03
BODYFORM
BODYFORM
78318569 not registered Dead/Abandoned
dela Chevrotiere, Ronald Jr., L.
2003-10-24
BODYFORM
BODYFORM
78182606 not registered Dead/Abandoned
Dreamwear Inc.
2002-11-07
BODYFORM
BODYFORM
77763714 3797387 Live/Registered
Brookstone Purchasing, Inc.
2009-06-19
BODYFORM
BODYFORM
77385035 3608202 Dead/Cancelled
PRECARE CORP.
2008-01-31
BODYFORM
BODYFORM
77225781 3578524 Live/Registered
Dreamwear Inc.
2007-07-10
BODYFORM
BODYFORM
76323005 not registered Dead/Abandoned
WARRIOR LACROSSE, INC.
2001-10-05
BODYFORM
BODYFORM
74427961 1985972 Dead/Cancelled
CUSTOMERS ARE REALLY EVERYTHING CORP.
1993-08-23
BODYFORM
BODYFORM
73684564 not registered Dead/Abandoned
WOODBRIDGE FOAM CORPORATION, THE
1987-09-16

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