TranS1

FDA UDI

Class II (US FDA UDI)

by Quandary Medical Llc

Identity

Trade Name: TranS1 FDA UDI
Generic Name: Vertebral body prosthesis FDA UDI
Device Name: AxiaLIF Plus 1-Level 15.5 mm Non-Distracting Rod, 40 mm Length FDA UDI
Model / Reference: TR1-2384 FDA UDI
Description: AxiaLIF Plus 1-Level 15.5 mm Non-Distracting Rod, 40 mm Length FDA UDI

Identifiers

Primary DI / UDI-DI: 00815361020006 FDA UDI
510(k) Number: K102334 FDA UDI
FDA Product Code: KWQ FDA UDI
GMDN Term: Vertebral body prosthesis FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 888.3060 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: Vertebral body prosthesis

TranS1 by Quandary Medical Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Vertebral body prosthesis.

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VERTE-STACK® Spinal System — MEDTRONIC SOFAMOR DANEK, INC. · Class II
CASCADIA™ Interbody System — K2M, INC. · Class II
CAPRI™ Corpectomy Cage System — K2M, INC. · Class II
Cascadia™ Interbody System — K2M, INC. · Class II

Cleared under the same submission

K102334 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Quandary Medical Llc

Sources (1)

FDA UDI 7a8fb185-8f92-4b22-8ed4-8e090131addb 34 fields · synced Jun 6, 2026