XCIX DESIGN, LLC

FDA Device Registration & Listing · Richmond, UT, US · Registration 3027201862

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3027201862
FEI Number
3027201862
Entity Name
XCIX DESIGN, LLC
City/State/Country
Richmond, UT, US
Establishment Address
253 S 200 W, Richmond, UT 84333, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
XCIX Design, LLC (Owner Number: 10087846)
Owner / Operator Contact Address
253 S 200 W, Richmond, UT 84333, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
ODP Intervertebral Fusion Device With Bone Graft, Cervical Orthopedic Class 2 888.3080 2023-04-19
MQP Spinal Vertebral Body Replacement Device Orthopedic Class 2 888.3060 2023-04-19

Official Correspondent

Kyle Atwood

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

XCIX Design, LLC
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K142269 Reliance Medical Systems, LLC Reliance Cervical IBF System 2015-06-09
K122085 Omni Surgical, LP Dba Spine360 STINGRAY CERVICAL CAGE 2012-10-17
K120275 Synthes (Usa), LLC SYNTHES ACIS/VERTEBRAL SPACER CR 2012-05-25
K041888 Signus Medizintechnik GmbH CURVED PEEK TETRIS SPINAL IMPLANT 2004-08-10
K211892 Arftx Medical, LLC ArtFx Corpectomy Cages (Espinax and Distractania Corpectomy Cages) 2022-10-06

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3027201862. Last updated year: 2026. Please use registration number 3027201862 when referencing this establishment in official correspondence.
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