Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3010083866

FEI Number

3010083866

Entity Name

PRECISION INC

City/State/Country

Minneapolis, MN, US

Establishment Address

1700 Freeway Blvd, Minneapolis, MN 55430, US

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Precision Inc (Owner Number: 10084549)

Owner / Operator Contact Address

1700 Freeway Blvd, Minneapolis, MN 55430, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Marker, Radiographic, Implantable EnVisio Navigation System Navigator

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
NEU	Marker, Radiographic, Implantable	General, Plastic Surgery	Class 2	878.4300	2022-03-04

Official Correspondent

Jamon Aaberg

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Precision Inc

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 3010083866. Last updated year: 2026. Please use registration number 3010083866 when referencing this establishment in official correspondence.