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Uni-Thread®

FDA UDI

Class II (US FDA UDI)

by Spine Vision, Inc.

Identity

Trade Name
UNI-THREAD® FDA UDI
Generic Name
Spinal bone screw, non-bioabsorbable FDA UDI
Device Name
Ti 6.5 mm x 28-33 mm screw with cylindrical post FDA UDI
Model / Reference
L2-C633T FDA UDI
Description
Ti 6.5 mm x 28-33 mm screw with cylindrical post FDA UDI

Identifiers

Primary DI / UDI-DI
03663136004778 FDA UDI
510(k) Number
K013301 FDA UDI
FDA Product Code
MNH FDA UDI
MNI FDA UDI
GMDN Term
Spinal bone screw, non-bioabsorbable 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

Yes

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

Category: Spinal bone screw, non-bioabsorbable

Uni-Thread® by Spine Vision, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Spinal bone screw, non-bioabsorbable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Spine Vision, Inc.

Sources (1)

  • FDA UDI 892f3e43-146f-47c5-ae0d-986f94a993e2 35 fields · synced May 30, 2026