← Back to catalogue

TILock

FDA UDI

Class II (US FDA UDI)

by Genesys Orthopedics Systems LLC

Identity

Trade Name
TILock FDA UDI
Generic Name
Bone-screw internal spinal fixation system, non-sterile FDA UDI
Device Name
5.0mm x 60mm TiLock Cortical Cannulated Low-Top Screw FDA UDI
Model / Reference
1 FDA UDI
Description
5.0mm x 60mm TiLock Cortical Cannulated Low-Top Screw FDA UDI

Identifiers

Catalog Number
G732-50-60 FDA UDI
Primary DI / UDI-DI
M719G73250600 FDA UDI
FDA Product Code
NKB FDA UDI
MNI FDA UDI
MNH 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
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
Length — 60 Millimeter FDA UDI
Outer Diameter — 5.0 Millimeter FDA UDI

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

TILock by Genesys Orthopedics Systems LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Genesys Orthopedics Systems LLC

Sources (1)

  • FDA UDI 8a203ded-3917-41c8-9f09-87c9516520e8 36 fields · synced Jun 6, 2026