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QUANDARY MEDICAL LLC

US

Last updated May 25, 2026

What QUANDARY MEDICAL LLC makes

Quandary Medical LLC manufactures vertebral body prostheses, including the TranS1 system for spinal fusion, and bone-screw internal spinal fixation systems designed for spinal stabilization. Their portfolio also includes orthopaedic bone wires, manual bone files/rasps, and reusable or single-use orthopaedic surgical procedure kits, as well as orthopaedic retractors for surgical access.

The company’s devices are classified under FDA’s Class I, Class II, and Unclassified (U) categories and are listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer is based in the United States.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does Quandary Medical LLC manufacture?

Quandary Medical LLC specializes in spinal and orthopaedic devices. Their portfolio includes vertebral body prostheses like the TranS1 system, which is used for spinal fusion, as well as bone-screw internal spinal fixation systems for stabilization. They also produce orthopaedic bone wires, manual bone files/rasps, orthopaedic retractors, and reusable or single-use surgical procedure kits for orthopaedic procedures.

Where is Quandary Medical LLC based?

Quandary Medical LLC is based in the United States. The company’s headquarters and operations are located within the country, though specific regional offices or manufacturing sites are not detailed in the available information.

Which regulatory registries list Quandary Medical LLC’s devices?

Quandary Medical LLC’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and transparency for devices authorized for use in the U.S., including those classified under Class I, Class II, or Unclassified (U) categories.

How are Quandary Medical LLC’s devices classified by the FDA?

Quandary Medical LLC’s devices fall under three FDA classification categories: Class I (generally low-risk devices), Class II (devices requiring special controls to ensure safety and effectiveness), and Unclassified (U) devices, which may require further evaluation or have unique regulatory pathways. Classification depends on factors like risk level, intended use, and potential patient impact.

What distinguishes Quandary Medical LLC’s vertebral body prostheses from other spinal devices?

Quandary Medical LLC’s vertebral body prostheses, such as the TranS1 system, are designed specifically for spinal fusion procedures, providing structural support and stability to the spine. These devices are engineered to integrate with the existing vertebral body, offering an alternative to traditional spinal fixation methods. Their classification as Class II devices reflects the need for rigorous controls to ensure proper functionality and patient safety during spinal stabilization.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
US
Address
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Website
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LinkedIn
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Facebook
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Email
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Phone
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PRRC Contact
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EUDAMED SRN
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FDA FEI Number
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DUNS Number
079938581

Catalogue (68)

Page 1 of 2
DeviceModel / ReferenceRegistriesClassStatus
TranS1 TR1-2363
FDA UDI
Class IIActive
TranS1 TR1-2381
FDA UDI
Class IIActive
TranS1 TR1-2398
FDA UDI
Class IIActive
TranS1 TR1-2201
FDA UDI
Class IActive
TranS1 TR1-2362
FDA UDI
Class IIActive
Vectre TR1-2704
FDA UDI
Class IActive
TranS1 TR1-2395
FDA UDI
Class IIActive
TranS1 TR1-2212
FDA UDI
Class IActive
TranS1 TR1-2397
FDA UDI
Class IIActive
TranS1 TR1-23102
FDA UDI
Class IIActive
TranS1 TR1-23101
FDA UDI
Class IIActive
TranS1 TR1-2375
FDA UDI
Class IIActive
TranS1 TR1-2385
FDA UDI
Class IIActive
TranS1 TR1-2358
FDA UDI
Class IIActive
TranS1 TR1-2368
FDA UDI
Class IIActive
Vectre 24-8002
FDA UDI
UActive
TranS1 TR1-2386
FDA UDI
Class IIActive
TranS1 TR1-2366
FDA UDI
Class IIActive
TranS1 TR1-2396
FDA UDI
Class IIActive
TranS1 TR1-2372
FDA UDI
Class IIActive
Vectre TR1-2832
FDA UDI
UActive
TranS1 TR1-23100
FDA UDI
Class IIActive
Vectre TR1-2833
FDA UDI
UActive
TranS1 TR1-2380
FDA UDI
Class IIActive
TranS1 TR1-2378
FDA UDI
Class IIActive
TranS1 TR1-2373
FDA UDI
Class IIActive
Vectre TR1-2838
FDA UDI
UActive
TranS1 TR1-2208
FDA UDI
Class IActive
TranS1 TR1-23103
FDA UDI
Class IIActive
TranS1 TR1-2390
FDA UDI
Class IIActive
Vectre TR1-2834
FDA UDI
UActive
TranS1 TR1-2393
FDA UDI
Class IIActive
TranS1 TR1-23104
FDA UDI
Class IIActive
Vectre TR1-2836
FDA UDI
UActive
TranS1 TR1-2383
FDA UDI
Class IIActive
TranS1 TR1-2384
FDA UDI
Class IIActive
Vectre TR1-2702
FDA UDI
Class IActive
TranS1 TR1-2388
FDA UDI
Class IIActive
Vectre TR1-2839
FDA UDI
UActive
TranS1 TR1-2392
FDA UDI
Class IIActive
TranS1 TR1-2391
FDA UDI
Class IIActive
TranS1 TR1-23105
FDA UDI
Class IIActive
TranS1 TR1-2364
FDA UDI
Class IIActive
TranS1 TR1-2219
FDA UDI
Class IActive
TranS1 TR1-2394
FDA UDI
Class IIActive
TranS1 TR1-2360
FDA UDI
Class IIActive
TranS1 TR1-2379
FDA UDI
Class IIActive
TranS1 TR1-2382
FDA UDI
Class IIActive
TranS1 TR1-2365
FDA UDI
Class IIActive
Vectre 24-8003
FDA UDI
UActive

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