Aurora Spine Manufacturing

FDA Device Registration & Listing · Carlsbad, CA, US · Registration 3020417298

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
3020417298
FEI Number
3020417298
Entity Name
Aurora Spine Manufacturing
City/State/Country
Carlsbad, CA, US
Establishment Address
3146 Tiger Run Ct, Suite 116, Carlsbad, CA 92010, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Aurora Spine (Owner Number: 10045511)
Owner / Operator Contact Address
1930 Palomar Point Way, Ste 103, Carlsbad, CA 92008, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

ZIP MIS Interspinous Fusion System ZIP ULTRA MIS Interspinous Fusion System SILO TFX

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
PEK Spinous Process Plate Orthopedic Class 2 888.3050 2013-12-13

Official Correspondent

Laszlo Garamszegi

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Aurora Spine
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3010326971 AURORA SPINE, INC. Carlsbad, CA, US

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3020417298. Last updated year: 2026. Please use registration number 3020417298 when referencing this establishment in official correspondence.
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