Not currently registered with FDA under this name

Tri-Stage, Inc.

San Diego, CA, United States. Named as applicant on 3 dental 510(k) clearances 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: 31988–1988
Markets registered in: 1United States
Establishments: 0—

510(k) clearances per year, 1980–2026

510(k) clearances

Clearances on which FDA names Tri-Stage, Inc. as the applicant.

Decided	510(k)	Device	Device type
2 Aug 1988	K882834	TISSUE PUNCH	EKJ Operative Burnisher
21 Jun 1988	K882183	DENTAL BURS	EJL Dental Bur
31 Mar 1988	K880220	TRI-STAGE (TS-I) DENTAL IMPLANT	DZE Root-Form Endosseous Implant

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.