Lantern Surgical Assistant 402519-05

GUDID 00810832031680

Microport Advance, Balance Drill Plate, Size 5

ORTHALIGN, INC.

Orthopaedic surgical procedure kit, non-medicated, reusable Orthopaedic surgical procedure kit, non-medicated, reusable Orthopaedic surgical procedure kit, non-medicated, reusable Orthopaedic surgical procedure kit, non-medicated, reusable Orthopaedic surgical procedure kit, non-medicated, reusable Orthopaedic surgical procedure kit, non-medicated, reusable Orthopaedic surgical procedure kit, non-medicated, reusable Orthopaedic surgical procedure kit, non-medicated, reusable Orthopaedic surgical procedure kit, non-medicated, reusable Orthopaedic surgical procedure kit, non-medicated, reusable Orthopaedic surgical procedure kit, non-medicated, reusable Orthopaedic surgical procedure kit, non-medicated, reusable Orthopaedic surgical procedure kit, non-medicated, reusable Orthopaedic surgical procedure kit, non-medicated, reusable Orthopaedic surgical procedure kit, non-medicated, reusable Orthopaedic surgical procedure kit, non-medicated, reusable Orthopaedic surgical procedure kit, non-medicated, reusable Orthopaedic surgical procedure kit, non-medicated, reusable
Primary Device ID00810832031680
NIH Device Record Key9ff33d4e-0b7e-49fd-9765-088326bd999e
Commercial Distribution StatusIn Commercial Distribution
Brand NameLantern Surgical Assistant
Version Model Number402519-05
Catalog Number402519-05
Company DUNS023266163
Company NameORTHALIGN, 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 Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone866-582-0879
Emailcustomerservice@orthalign.com
Phone866-582-0879
Emailcustomerservice@orthalign.com
Phone866-582-0879
Emailcustomerservice@orthalign.com
Phone866-582-0879
Emailcustomerservice@orthalign.com
Phone866-582-0879
Emailcustomerservice@orthalign.com
Phone866-582-0879
Emailcustomerservice@orthalign.com
Phone866-582-0879
Emailcustomerservice@orthalign.com
Phone866-582-0879
Emailcustomerservice@orthalign.com
Phone866-582-0879
Emailcustomerservice@orthalign.com
Phone866-582-0879
Emailcustomerservice@orthalign.com
Phone866-582-0879
Emailcustomerservice@orthalign.com
Phone866-582-0879
Emailcustomerservice@orthalign.com
Phone866-582-0879
Emailcustomerservice@orthalign.com
Phone866-582-0879
Emailcustomerservice@orthalign.com
Phone866-582-0879
Emailcustomerservice@orthalign.com
Phone866-582-0879
Emailcustomerservice@orthalign.com
Phone866-582-0879
Emailcustomerservice@orthalign.com
Phone866-582-0879
Emailcustomerservice@orthalign.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100810832031680 [Primary]

FDA Product Code

OLOOrthopedic Stereotaxic Instrument

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00810832031680]

Moist Heat or Steam Sterilization

[00810832031680]

Moist Heat or Steam Sterilization

[00810832031680]

Moist Heat or Steam Sterilization

[00810832031680]

Moist Heat or Steam Sterilization

[00810832031680]

Moist Heat or Steam Sterilization

[00810832031680]

Moist Heat or Steam Sterilization

[00810832031680]

Moist Heat or Steam Sterilization

[00810832031680]

Moist Heat or Steam Sterilization

[00810832031680]

Moist Heat or Steam Sterilization

[00810832031680]

Moist Heat or Steam Sterilization

[00810832031680]

Moist Heat or Steam Sterilization

[00810832031680]

Moist Heat or Steam Sterilization

[00810832031680]

Moist Heat or Steam Sterilization

[00810832031680]

Moist Heat or Steam Sterilization

[00810832031680]

Moist Heat or Steam Sterilization

[00810832031680]

Moist Heat or Steam Sterilization

[00810832031680]

Moist Heat or Steam Sterilization

[00810832031680]

Moist Heat or Steam Sterilization

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-09-11
Device Publish Date2023-09-01

On-Brand Devices [Lantern Surgical Assistant]

00810832031635JOURNEY II SIZES 9-10 DRILL PLATE
00810832031628JOURNEY II SIZES 7-8 DRILL PLATE
00810832031611JOURNEY II SIZES 5-6 DRILL PLATE
00810832031604JOURNEY II SIZES 3-4 DRILL PLATE
00810832031598JOURNEY II SIZES 1-2 DRILL PLATE
00810832031864Drill Plate, United Orthopedics, Size 1-7
00810832031857Drill Plate, Lima Physica, Size 1-10
00810832031840Drill Plate, Globus GENflex2, Posterior Ref Size 1-6
00810832031819Microport Evolution PR, Balance Drill Plate, Sizes 5-7
00810832031802Microport Evolution PR, Balance Drill Plate, Sizes 1-4
00810832031789Microport Evolution DCF, Balance Drill Plate, Size 8
00810832031772Microport Evolution DCF, Balance Drill Plate, Size 7
00810832031765Microport Evolution DCF, Balance Drill Plate, Size 6
00810832031758Microport Evolution DCF, Balance Drill Plate, Size 5
00810832031741Microport Evolution DCF, Balance Drill Plate, Size 4
00810832031734Microport Evolution DCF, Balance Drill Plate, Size 3
00810832031727Microport Evolution DCF, Balance Drill Plate, Size 2
00810832031710Microport Evolution DCF, Balance Drill Plate, Size 1
00810832031697Microport Advance, Balance Drill Plate, Size 6
00810832031680Microport Advance, Balance Drill Plate, Size 5
00810832031673Microport Advance, Balance Drill Plate, Size 4
00810832031666Microport Advance, Balance Drill Plate, Size 3
00810832031659Microport Advance, Balance Drill Plate, Size 2
00810832031642Microport Advance, Balance Drill Plate, Size 1
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