PINTA ELEMENTS

FDA Device Registration & Listing · Minneapolis, MN, US · Registration 3009230570

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
3009230570
FEI Number
3009230570
Entity Name
PINTA ELEMENTS
City/State/Country
Minneapolis, MN, US
Establishment Address
2601 49th Ave N, Suite 400, Minneapolis, MN 55430, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
pinta elements (Owner Number: 10056596)
Owner / Operator Contact Address
2601 49th Ave N, Suite 400, Minneapolis, MN 55430, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Bone Foam

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
IQI Orthosis, Limb Brace Physical Medicine Class 1 890.3475 2022-07-26

Official Correspondent

Nadine Gieschen

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

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

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3009230570. Last updated year: 2026. Please use registration number 3009230570 when referencing this establishment in official correspondence.
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