FDA.reportPublic FDA data

ION Disposable Instrument Kit

Primary DI
00810131881795
Brand
ION Disposable Instrument Kit
Company
Surgentec, LLC
Model
TI-K-1000
Published
2026-03-09
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
OTC
false
Sterile
true
Single use
true

Product Codes#

Code, Name table
CodeName
MRWSystem, Facet Screw Spinal Device

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
MRWSystem, Facet Screw Spinal DeviceUnknownU

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K241416000
K243265000
K261209000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K241416000Ion 3DSurGenTec, LLC2024-06-17MRW
K243265000Ion 3DSurGenTec, LLC2024-12-04MRW
K261209000Ion-LSurGenTec, LLC2026-06-11MRW

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00810131881795PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00810131881795008101318817958101318817950810131881795

GMDN Terms#

Term, Definition table
TermDefinition
Facet joint prosthesisA sterile implantable device intended to resurface and/or replace a degenerative or otherwise diseased vertebral facet (apophyseal, zygapophyseal) joint. It typically consists of small plate-like metal [e.g., titanium (Ti), cobalt-chrome (Co-Cr)] device intended to be fixed to the superior and inferior articulating surfaces of the joint. Fixation may be by means of a trans-laminar or trans-facet screw or bolt.

Regulatory Flags#

DUNS number
004095409
Device count
1
DM exempt
false
Premarket exempt
false
HCT/P
false
Kit
false
Combination product
false
Lot or batch
true
Serial number
true
Manufacturing date on label
true
Expiration date on label
true
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
false
Sterilization required before use
false

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00810131884055TiLink-L Rescue Drill GuideSR21-27002026-09-25
00810131884062TiLink-L Rescue DilatorSR21-67012026-09-25
00810131884079TiLink-L Rescue Impact CapSR21-67022026-09-25
00810131884086TiLink-L Rescue screw Drill bit – 10.5mmSR21-67032026-09-25
00810131884857TiLink-L Sterilization Tray – Double StackSR21-70202026-09-25
00810131884864TiLink-L Rescue CaddySR21-70212026-09-25
00810131882983BMAN BCOR Bone Marrow Aspirate KitAAN-09-BCORES2026-08-19
00810131884697BMAN BCOR Bone Marrow Aspirate Kit (with Clip)AAN-09-BCORE2026-08-19
00810131885045ION Non CervicalSR17-10002026-07-28
00810131881801ION 55 Facet Implant - SterileTI-K-552026-03-09
00810131881818ION 60 Facet Implant - SterileTI-K-602026-03-09
00810131881825ION 65 Facet Implant - SterileTI-K-652026-03-09
00810131882433ION-C Navigation LocatorSR12-25122026-07-06
00810131882440Ion Navigation Drill Bit - 5.0mmSR12-65102026-07-06
00810131882457Ion Navigation Drill Bit - 5.5mmSR12-65112026-07-06
00810131882464Ion Navigation Drill Bit - 4.5mmSR12-65092026-07-06
00810131882532TiLink-L Navigation Drill Bit - 8mmSR21-63052026-07-06
00810131882556TiLink-L Navigation Drill GuideSR21-63012026-07-06
00810131882563TiLink-L Navigation Inserter Hexalobe DriverSR21-63042026-07-06
00810131882617TiLink-L Navigation Impact CapSR21-63032026-07-06

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Primary DI, Brand, Company table
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00888867614611Arthrex®ARTHREX, INC.MRW2026-10-07
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00888867614741Arthrex®ARTHREX, INC.MRW2026-10-07
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00888867614765Arthrex®ARTHREX, INC.MRW2026-10-07
00888867614772Arthrex®ARTHREX, INC.MRW2026-10-07
00888867614789Arthrex®ARTHREX, INC.MRW2026-10-07
00888867614796Arthrex®ARTHREX, INC.MRW2026-10-07
00888867614802Arthrex®ARTHREX, INC.MRW2026-10-07
00888867614819Arthrex®ARTHREX, INC.MRW2026-10-07
00888867614826Arthrex®ARTHREX, INC.MRW2026-10-07
00888867614833Arthrex®ARTHREX, INC.MRW2026-10-07