Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3027060896

FEI Number

3027060896

Entity Name

PERIOVIEW, LLC

City/State/Country

Surprise, AZ, US

Establishment Address

12425 W Bell Rd Ste C110, Surprise, AZ 85378, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

PerioView, LLC (Owner Number: 10087774)

Owner / Operator Contact Address

12425 W Bell road, C110, Surprise, AZ 85378, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Perio-View Periodntal lEndoscopic Therapy (P.E.T.) iEnvision PerioView If You Can't See it, You Can't Treat It Perioscope Perioscope iEnvision If You Can't See it, You Can't Treat It Periodntal lEndoscopic Therapy (P.E.T.) PerioView

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
NRD	Unit, Operative Dental, Accessories	Dental	Class 1	872.6640	2023-04-07
FWL	Camera, Cine, Endoscopic, Without Audio	General, Plastic Surgery	Class 1	878.4160	2023-04-07
FWD	Camera, Television, Microsurgical, Without Audio	General, Plastic Surgery	Class 1	878.4160	2024-03-28

Official Correspondent

Michael Austin

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

PerioView, LLC

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 3027060896. Last updated year: 2026. Please use registration number 3027060896 when referencing this establishment in official correspondence.