Not currently registered with FDA under this name

Branemark Integration AB

Goteborg, Sweden. Named as applicant on 3 dental 510(k) clearances between 2002 and 2009. No establishment is registered with FDA under this exact name today.

Device types listed: 0
Brands and models: 0
510(k) clearances: 32002–2009
Markets registered in: 1United States
Establishments: 0—

510(k) clearances per year, 2000–2026

510(k) clearances

Clearances on which FDA names Branemark Integration AB as the applicant.

Decided	510(k)	Device	Device type
19 May 2009	K090005	BRANEMARK INTEGRATION BIOHELIX IMPLANTS	DZE Root-Form Endosseous Implant
7 Apr 2004	K040643	BRANEMARK INTEGRATION DENTAL IMPLANT AND ACCESSORIES	DZE Root-Form Endosseous Implant
30 Aug 2002	K021355	ENDOSSEOUS 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.