BLT 4.1MM RC, SLACTIVE 10MM, TIZR, NTP

ENDOSSEOUS DENTAL IMPLANT

This device is manufactured by INSTITUT STRAUMANN AG.

The following problems were reported about this device:

Year	Description	Events/year	Type
2024	Unspecified Infection	232	Patient
2024	Swelling/ Edema	87	Patient
2024	Sinus Perforation	3	Patient
2024	Pain	315	Patient
2024	Numbness	4	Patient
2024	Inflammation	102	Patient
2024	Increased Sensitivity	33	Patient
2024	Hypersensitivity/Allergic reaction	10	Patient
2024	Hemorrhage/Blood Loss/Bleeding	50	Patient
2024	Fistula	43	Patient
2024	Fibrosis	540	Patient
2024	Abscess	28	Patient
2024	Loss of Osseointegration	238	Device
2024	Fracture	6	Device
2024	Failure to Osseointegrate	830	Device
2024	Difficult to Insert	7	Device
2024	Adverse Event Without Identified Device or Use Problem	49	Device
2023	Unspecified Infection	961	Patient
2023	Swelling/ Edema	372	Patient
2023	Sinus Perforation	29	Patient
2023	Pain	1334	Patient
2023	Numbness	26	Patient
2023	Inflammation	501	Patient
2023	Increased Sensitivity	183	Patient
2023	Hypersensitivity/Allergic reaction	66	Patient
2023	Hemorrhage/Blood Loss/Bleeding	306	Patient
2023	Fistula	146	Patient
2023	Fibrosis	2405	Patient
2023	Abscess	176	Patient
2023	Separation Failure	14	Device
2023	Loss of Osseointegration	1303	Device
2023	Fracture	47	Device
2023	Failure to Osseointegrate	4367	Device
2023	Difficult to Insert	51	Device
2023	Adverse Event Without Identified Device or Use Problem	549	Device
2022	Unspecified Infection	548	Patient
2022	Swelling/ Edema	271	Patient
2022	Sinus Perforation	21	Patient
2022	Pain	763	Patient
2022	Numbness	14	Patient
2022	Inflammation	320	Patient
2022	Increased Sensitivity	123	Patient
2022	Hypersensitivity/Allergic reaction	35	Patient
2022	Hemorrhage/Blood Loss/Bleeding	208	Patient
2022	Fistula	106	Patient
2022	Fibrosis	1434	Patient
2022	Abscess	90	Patient
2022	Separation Failure	24	Device
2022	Loss of Osseointegration	2712	Device
2022	Fracture	79	Device
2022	Failure to Osseointegrate	9508	Device
2022	Difficult to Insert	159	Device
2022	Adverse Event Without Identified Device or Use Problem	1212	Device
2021	Unspecified Infection	21	Patient
2021	Swelling/ Edema	3	Patient
2021	Pain	12	Patient
2021	Inflammation	2	Patient
2021	Hypersensitivity/Allergic reaction	2	Patient
2021	Hemorrhage/Blood Loss/Bleeding	9	Patient
2021	Fibrosis	25	Patient
2021	Abscess	1	Patient
2021	Loss of Osseointegration	207	Device
2021	Fracture	3	Device
2021	Failure to Osseointegrate	789	Device
2021	Difficult to Insert	4	Device
2021	Adverse Event Without Identified Device or Use Problem	51	Device
2020	Unspecified Infection	7	Patient
2020	Swelling/ Edema	1	Patient
2020	Sinus Perforation	1	Patient
2020	Pain	4	Patient
2020	Inflammation	3	Patient
2020	Increased Sensitivity	1	Patient
2020	Hypersensitivity/Allergic reaction	2	Patient
2020	Fibrosis	12	Patient
2020	Abscess	4	Patient
2020	Loss of Osseointegration	12	Device
2020	Failure to Osseointegrate	50	Device
2020	Difficult to Insert	1	Device