Not currently registered with FDA under this name

Zinnanti Surgical Instruments, Inc.

Chatsworth, CA, United States. Named as applicant on 3 dental 510(k) clearances between 1989 and 1989. No establishment is registered with FDA under this exact name today.

Device types listed: 0
Brands and models: 0
510(k) clearances: 31989–1989
Markets registered in: 22 registrations outside the US
Establishments: 0—

510(k) clearances per year, 1980–2026

Registered in 2 markets

Where regulators' registries name Zinnanti Surgical Instruments, Inc. 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	Zinnanti Surgical Instruments, Inc.	3 clearances	1989–1989	Below
Taiwan	TFDA	Manufacturer	ZINNANTI SURGICAL INSTRUMENTS INC	2	1985–1985	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 Zinnanti Surgical Instruments, Inc. as the applicant.

Decided	510(k)	Device	Device type
10 May 1989	K892261	RUBBER DAM CLAMPS/FORCEPS	EKJ Operative Burnisher
2 May 1989	K892260	PRICHARD PERIOSTEAL RETRACTOR #3	EKJ Operative Burnisher
1 May 1989	K892255	DENTAL ROOT ELEVATOR	EKO Denture Preformed (Partially Prefabricated Denture)

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.