Not currently registered with FDA under this name

Percussionaire Corp.

Sandpoint, ID, United States. Named as applicant on 1 dental 510(k) clearance between 1990 and 1990. No establishment is registered with FDA under this exact name today.

Device types listed: 0
Brands and models: 0
510(k) clearances: 11990–1990
Markets registered in: 724 registrations outside the US
Establishments: 0—

510(k) clearances per year, 1990–2026

Registered in 7 markets

Where regulators' registries name Percussionaire Corp. as the manufacturer or the registration holder of a device.

All markets

RegisteredHome: United StatesOne marker per market

Market	Regulator	Named as	Name on the registry	Registrations	Issued	Records
United States	FDA	Applicant	Percussionaire Corp.	1 clearances	1990–1990	Below
Canada	Health Canada	Registration holder	PERCUSSIONAIRE CORPORATION	13	2000–2010	Pure Global AI
Australia	TGA	Manufacturer	Percussionaire Corporation	3	2025–2025	Pure Global AI
European Union	EUDAMED	Manufacturer	Percussionaire Corporation	3	—	Pure Global AI
Costa Rica	Ministerio de Salud	Manufacturer	PERCUSSIONAIRE CORP.Percussionaire Corp	2	—	Pure Global AI
Japan	PMDA	Registration holder	Ｐｅｒｃｕｓｓｉｏｎａｉｒｅ　Ｃｏｒｐｏｒａｔｉｏｎ	2	2014–2015	Pure Global AI
Brazil	ANVISA	Manufacturer	PERCUSSIONAIRE CORPORATION	1	2011–2011	Pure Global AI

Outside the US the count is of all the company's device registrations in that market, dental or not · matched by company name and country · registry data read 12 Nov 2026

510(k) clearances

Clearances on which FDA names Percussionaire Corp. as the applicant.

Decided	510(k)	Device	Device type
9 Jan 1990	K896586	RATE INCREASE FOR IPPB/IPV	DZD Orthodontic Tube

Sources

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 of the most recent filing, which can be a US agent.