Adcura, Inc.

FDA Device Registration & Listing · Minnetonka, MN, US · Registration 3013758617

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
3013758617
FEI Number
3013758617
Entity Name
Adcura, Inc.
City/State/Country
Minnetonka, MN, US
Establishment Address
5959 Baker Rd Ste 340, Minnetonka, MN 55345, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility,Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device
Owner / Operator
ADCURA, INC. (Owner Number: 10059466)
Owner / Operator Contact Address
5959 BAKER RD STE 340, Minnetonka, MN 55345, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K181531
PMA Number
N/A

All Registered Proprietary Names

Sagittae® Sagittae Sagittae

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
MAX Intervertebral Fusion Device With Bone Graft, Lumbar Orthopedic Class 2 888.3080 2022-12-19
OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar Orthopedic Class 2 888.3080 2019-03-07
MAX Intervertebral Fusion Device With Bone Graft, Lumbar Orthopedic Class 2 888.3080 2019-03-07
MAX Intervertebral Fusion Device With Bone Graft, Lumbar Orthopedic Class 2 888.3080 2019-01-28
OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar Orthopedic Class 2 888.3080 2019-01-28

Official Correspondent

ANDREW ROGERS

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

ADCURA, INC.
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
K223430 Life Spine, Inc. ProLift Micro Expandable Spacer System 2023-05-04
K102293 Globus Medical, Inc. CALIBER SPACER 2011-01-05
K193541 Nu Vasive, Incorporated NuVasive Cohere Thoracolumbar Interbody System 2020-03-30
K080401 Advanced Medical Technologies AG SHELL CAGE, WAVE CAGE, LOOP CAGE 2008-05-09
K200084 Zavation Medical Products, LLC Zavation IBF System 2020-10-19

Similar Registrations

Registration Number Establishment Name Location
3021588295 XYRESIC LLC Jackson, MI, US
3017936978 CARLSMED, INC. Carlsbad, CA, US
3016050940 Olive Branch Distribution Center Olive Branch, MS, US
2134947 GAUTHIER BIOMEDICAL, INC. Grafton, WI, US
1526534 Sterigenics US, LLC Lewis Center, OH, US
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3013758617. Last updated year: 2026. Please use registration number 3013758617 when referencing this establishment in official correspondence.
Legal Disclaimer: AvaSpecs is not affiliated with the FDA or any government agency and does not provide medical, legal, regulatory, safety, approval, clearance, effectiveness, endorsement, or compliance advice. This index page is built using public record archives and does not represent an official regulatory determination.
Account Required Full available specs will require a free AvaSpecs account.