Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3010610937

FEI Number

3010610937

Entity Name

PRECEPTIS MEDICAL, INC

City/State/Country

Golden Valley, MN, US

Establishment Address

8401 Wayzata Blvd, Suite 110, Golden Valley, MN 55426, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility,Manufacture Medical Device

Owner / Operator

Preceptis Medical Inc. (Owner Number: 10045707)

Owner / Operator Contact Address

8401 Wayzata Blvd, Suite 110, Golden Valley, MN 55426, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K133921

PMA Number

N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
ETD	Tube, Tympanostomy	Ear, Nose, Throat	Class 2	874.3880	2022-08-03

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Preceptis Medical Inc.

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Similar Registrations

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3018094310	Medtronic Engineering and Innovation Center (MEIC)	Hyderabad Telangana, IN
3010132111	Synergy Health Sterilisation UK Ltd	Swindon Wiltshire, GB

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010610937. Last updated year: 2026. Please use registration number 3010610937 when referencing this establishment in official correspondence.