FDA.reportPublic FDA data

PointCloud Knee Instruments

Primary DI
TKRR0001L0890
Brand
PointCloud Knee Instruments
Company
Unik Orthopedics Inc.
Model
UKI0201-R
Device description
UNIKO PointCloud Knee Instrument Kit
Published
2026-05-05
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
Single use
true

Product Codes#

Code, Name table
CodeName
JWHProsthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
LLZSystem, Image Processing, Radiological
MBHProsthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer
OOGKnee Arthroplasty Implantation System

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
JWHProsthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/PolymerOrthopedic2
LLZSystem, Image Processing, RadiologicalRadiology2
MBHProsthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/PolymerOrthopedic2
OOGKnee Arthroplasty Implantation SystemOrthopedic2

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
TKRR0001L0890PrimaryHIBCC0

GMDN Terms#

Term, Definition table
TermDefinition
Total knee prosthesis implantation guide-instrument kitA collection of sterile hand-held surgical instruments intended to be used during total knee arthroplasty (TKA), either manually or as a computer-assisted surgery (CAS) device, to aid in the navigation/placement of the prosthesis or other instruments. Components may be used for the following applications: 1) to hold/align/fix bone preparation instruments, prosthesis, or prosthesis component; 2) to provide relative position landmarks; 3) to ascertain correct spatial orientation or limb alignment; and/or 4) as an interface between prosthesis components; the implant is not included. This is a single-use device.

Sterilization Methods#

Method table
Method
Moist Heat or Steam Sterilization

Regulatory Flags#

DUNS number
118205691
Device count
1
Serial number
true
Manufacturing date on label
true
Expiration date on label
true
Sterilization required before use
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
TKRL000173910PointCloud Knee InstrumentsUKI0201-L2026-05-05
TKRL0001971B0PointCloud Knee InstrumentsUKI0201-L2026-05-05
TKRL0001B33I0PointCloud Knee InstrumentsUKI0201-L2026-05-05
TKRL0001B7250PointCloud Knee InstrumentsUKI0201-L2026-05-05
TKRL0001B9L20PointCloud Knee InstrumentsUKI0201-L2026-05-05
TKRL0001BK980PointCloud Knee InstrumentsUKI0201-L2026-05-05
TKRL0001BLF60PointCloud Knee InstrumentsUKI0201-L2026-05-05
TKRL0001D0L90PointCloud Knee InstrumentsUKI0201-L2026-05-05
TKRL0001D1B10PointCloud Knee InstrumentsUKI0201-L2026-05-05
TKRL0001D2DB0PointCloud Knee InstrumentsUKI0201-L2026-05-05
TKRL0001D3410PointCloud Knee InstrumentsUKI0201-L2026-05-05
TKRL0001D46I0PointCloud Knee InstrumentsUKI0201-L2026-05-05
TKRL0001D4KF0PointCloud Knee InstrumentsUKI0201-L2026-05-05
TKRL0001D5990PointCloud Knee InstrumentsUKI0201-L2026-05-05
TKRL0001D6KI0PointCloud Knee InstrumentsUKI0201-L2026-05-05
TKRL0001D8540PointCloud Knee InstrumentsUKI0201-L2026-05-05
TKRL0001DBD90PointCloud Knee InstrumentsUKI0201-L2026-05-05
TKRL0001DDKK0PointCloud Knee InstrumentsUKI0201-L2026-05-05
TKRL0001DFK60PointCloud Knee InstrumentsUKI0201-L2026-05-05
TKRL0001DIID0PointCloud Knee InstrumentsUKI0201-L2026-05-05

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
M722CP26183V261830ClearRead CT Platform DockerRiverain Technologies, Inc.LLZ2026-07-17
00854393006084VelocityVARIAN MEDICAL SYSTEMS, INC.LLZ2026-07-16
00885556923023NASmith & Nephew, Inc.JWH2026-07-16
05060737370000CaRi-PlaqueCARISTO DIAGNOSTICS LIMITEDLLZ2026-01-05
00866463000465STAGESpintech, Inc.LLZ2025-03-27
B228INTELEHEART0InteleHeartLes Systèmes Médicaux Intelerad IncorporéeLLZ2024-05-16
07649990819006OsiriX MDPixmeo SàrlLLZ2022-02-19
08800017262178EXULT Knee Replacement SystemCorentec Co., LtdJWH2020-01-10
08800017262185EXULT Knee Replacement SystemCorentec Co., LtdJWH2020-01-10
08800017262192EXULT Knee Replacement SystemCorentec Co., LtdJWH2020-01-10
08800017262208EXULT Knee Replacement SystemCorentec Co., LtdJWH2020-01-10
08800017262215EXULT Knee Replacement SystemCorentec Co., LtdJWH2020-01-10
08800017262222EXULT Knee Replacement SystemCorentec Co., LtdJWH2020-01-10
08800017262239EXULT Knee Replacement SystemCorentec Co., LtdJWH2020-01-10
08800017262246EXULT Knee Replacement SystemCorentec Co., LtdJWH2020-01-10
08800017262253EXULT Knee Replacement SystemCorentec Co., LtdJWH2020-01-10
08800017262260EXULT Knee Replacement SystemCorentec Co., LtdJWH2020-01-10
08800017262277EXULT Knee Replacement SystemCorentec Co., LtdJWH2020-01-10
08800017262284EXULT Knee Replacement SystemCorentec Co., LtdJWH2020-01-10
08800017262291EXULT Knee Replacement SystemCorentec Co., LtdJWH2020-01-10
08800017262307EXULT Knee Replacement SystemCorentec Co., LtdJWH2020-01-10
08800017262314EXULT Knee Replacement SystemCorentec Co., LtdJWH2020-01-10
08800017262321EXULT Knee Replacement SystemCorentec Co., LtdJWH2020-01-10
08800017262338EXULT Knee Replacement SystemCorentec Co., LtdJWH2020-01-10
08800017262345EXULT Knee Replacement SystemCorentec Co., LtdJWH2020-01-10
08800017262352EXULT Knee Replacement SystemCorentec Co., LtdJWH2020-01-10
08800017262369EXULT Knee Replacement SystemCorentec Co., LtdJWH2020-01-10
08800017262376EXULT Knee Replacement SystemCorentec Co., LtdJWH2020-01-10
08800017262383EXULT Knee Replacement SystemCorentec Co., LtdJWH2020-01-10
08800017262390EXULT Knee Replacement SystemCorentec Co., LtdJWH2020-01-10