TeKForce

Primary DI
00810198920352
Brand
TeKForce
Company
TheraMicro, LLC
Model
2471K012
Device description
TeKForce 1.2mm All-Suture Anchor Instrument Kit
Published
2026-08-18
Public version status
New
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
LXHOrthopedic Manual Surgical Instrument

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
LXHOrthopedic Manual Surgical InstrumentOrthopedic1

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00810198920352PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00810198920352008101989203528101989203520810198920352

GMDN Terms#

Term, Definition table
TermDefinition
Orthopaedic surgical procedure kit, non-medicated, single-useA collection of various sterile orthopaedic surgical instruments, dressings, and other materials intended to be used to perform an orthopaedic surgical procedure, however the kit is not dedicated to orthopaedic implantation. It does not contain pharmaceuticals. This is a single-use device.

Regulatory Flags#

DUNS number
133029114
Device count
1
DM exempt
false
Premarket exempt
true
HCT/P
false
Kit
false
Combination product
false
Lot or batch
true
Serial number
false
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
00810198920345General Instruments2509DK502026-08-18
00810198920376TeKForce2514K0012026-08-18
00810198920178TeKBrace2509K0322026-08-14
00810198920086TekBrace2470K0122026-04-17
00810198920093TekBrace2470K0252026-04-17
00810198920109TekBrace2508K0082026-04-17
00810198920116TekBrace2470E3902026-04-17
00810198920123TekBrace2470E4752026-04-17
00810198920130TekBrace Solo2508S0082026-04-17
00810198920147TekBrace2470A3902026-04-17
00810198920154TekBrace2470A4752026-04-17
00810198920161TekBrace2470A5502026-04-17
00810198920222TekBrace2470K2122026-04-17
00810198920239TekBrace2470K2252026-04-17
00810198920246TekBrace2513K1252026-04-17
00810198920253TekBrace2509K0252026-04-17
00810198920260TekBrace2470E5502026-04-17
00810198920307TeKForce2471A0122026-04-17
00810198920314TeKForce2471A0152026-04-17
00810198920321TeKForce2471A1152026-04-17

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
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00840606185967ALIFSPINAL ELEMENTS, INC.LXH2026-08-26
00840606185974ALIFSPINAL ELEMENTS, INC.LXH2026-08-26
00840606185981ALIFSPINAL ELEMENTS, INC.LXH2026-08-26
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00840606186001ALIFSPINAL ELEMENTS, INC.LXH2026-08-26
00840606186018ALIFSPINAL ELEMENTS, INC.LXH2026-08-26
00840606186025ALIFSPINAL ELEMENTS, INC.LXH2026-08-26
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00840606186049ALIFSPINAL ELEMENTS, INC.LXH2026-08-26
00840606186056ALIFSPINAL ELEMENTS, INC.LXH2026-08-26
00840606186063ALIFSPINAL ELEMENTS, INC.LXH2026-08-26
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00840606186100ALIFSPINAL ELEMENTS, INC.LXH2026-08-26
00840606186117ALIFSPINAL ELEMENTS, INC.LXH2026-08-26
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00840606186131ALIFSPINAL ELEMENTS, INC.LXH2026-08-26
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00840606186155ALIFSPINAL ELEMENTS, INC.LXH2026-08-26
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00840606186209ALIFSPINAL ELEMENTS, INC.LXH2026-08-26
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