ORTHOASCENT LLC

FDA Device Registration & Listing · Westminster, CO, US · Registration 3032542289

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
3032542289
FEI Number
3032542289
Entity Name
ORTHOASCENT LLC
City/State/Country
Westminster, CO, US
Establishment Address
9035 Wadsworth Pkwy Ste 1000, Westminster, CO 80021, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198,Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
OrthoAscent LLC (Owner Number: 10091190)
Owner / Operator Contact Address
9035 Wadsworth Pkwy #1000, Westminster, CO 80021, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
BK241083
PMA Number
N/A

All Registered Proprietary Names

Ascent Flexx BMC Ascent Flexx PRP

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
JQC Centrifuges (Micro, Ultra, Refrigerated) For Clinical Use Clinical Chemistry Class 1 862.2050 2024-09-30
ORG Platelet And Plasma Separator For Bone Graft Handling Hematology Class 2 864.9245 2024-09-30

Official Correspondent

Mike Masters

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

OrthoAscent LLC
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3032542289. Last updated year: 2026. Please use registration number 3032542289 when referencing this establishment in official correspondence.
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