Not currently registered with FDA under this name

Storz Instrument Co.

St. Louis, MO, United States. Named as applicant on 1 dental 510(k) clearance between 1988 and 1988. No establishment is registered with FDA under this exact name today.

Device types listed: 0
Brands and models: 0
510(k) clearances: 11988–1988
Markets registered in: 212 registrations outside the US
Establishments: 0—

510(k) clearances per year, 1980–2026

Registered in 2 markets

Where regulators' registries name Storz Instrument Co. 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	Storz Instrument Co.	1 clearances	1988–1988	Below
Taiwan	TFDA	Manufacturer	STORZ INSTRUMENT COMPANY	12	1980–1993	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 Storz Instrument Co. as the applicant.

Decided	510(k)	Device	Device type
19 Feb 1988	K873926	STORZ CONTOURED ANATOMICAL PLATING INSTRUMENT	JEY Bone Plate

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.