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TIGER Spine OCT System

FDA UDI

Class II (US FDA UDI)

by Corelink Llc

Identity

Trade Name
TIGER Spine OCT System FDA UDI
Generic Name
Bone-screw internal spinal fixation system, non-sterile FDA UDI
Device Name
3500 SERIES PRE-BENT ROD - COBALT CHROME WITH LINE - 3.5MM X 75MM FDA UDI
Model / Reference
R3503-075 FDA UDI
Description
3500 SERIES PRE-BENT ROD - COBALT CHROME WITH LINE - 3.5MM X 75MM FDA UDI

Identifiers

Catalog Number
R3503-075 FDA UDI
Primary DI / UDI-DI
M725R3503075 FDA UDI
FDA Product Code
MNH FDA UDI
KWP FDA UDI
MNI FDA UDI
GMDN Term
Bone-screw internal spinal fixation system, non-sterile FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3070 FDA UDI
888.3050 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 3.5 Millimeter FDA UDI
Length — 75 Millimeter FDA UDI

Category: Bone-screw internal spinal fixation system, non-sterile

The TIGER Spine OCT System is a comprehensive spinal fixation solution designed for orthopedic procedures. It offers a unique combination of internal and external fixation methods, making it an ideal choice for treating various spinal instabilities or deformities.

Similar devices

Also classified as Bone-screw internal spinal fixation system, non-sterile.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Corelink Llc

Sources (1)

  • FDA UDI 84354132-bea3-4e7c-b3c8-3d0773a56125 36 fields · synced Jul 14, 2026