Manufacturer registered with FDA

PerioView, LLC

Surprise, AZ, United States. Lists 1 dental device type with FDA across 1 registered establishment, and holds 1 510(k) clearance as applicant.

FDA owner/operator10087774Manufacturer

Device types listed: 1
Brands and models: 1
510(k) clearances: 11995–1995
Markets registered in: 1United States
Establishments: 1United States

510(k) clearances per year, 1990–2026

Devices listed with FDA

What PerioView, LLC currently lists, by FDA device type, with the brand and model names on the listing.

Device type	Category	Role	Brands and models	Listed since
Accessories Operative Dental UnitNRD · Class 1	—	Maker	Perio-View	2023

Source: FDA establishment registration & device listing, 510(k) and product classification files · FDA data as of 2 Nov 2026 · snapshot 12 Nov 2026

510(k) clearances

Clearances on which FDA names PerioView, LLC as the applicant.

Decided	510(k)	Device	Device type
15 Nov 1995	K953912	JACOBYSCOPE	EIA Operative Dental Unit

Registered establishments

Establishment	Location	What it does
PERIOVIEW, LLCFDA reg. 3027060896	Surprise, AZ, United States	Manufacturer

Sources

FDA establishment registration & device listing (search FDA, owner/operator 10087774). FDA 510(k) premarket notification file. FDA data as of 2 Nov 2026; snapshot 12 Nov 2026. The location shown is the address on FDA's record.