ClearanceBrief
Company

mo-Vis BVBA

FDA 510(k) clearances and medical device recalls filed under this name. Name variants (Inc, Corp, punctuation) are merged.

0510(k) clearances (0 in 12 months)
7recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
KNNComponents, Wheelchair7

Latest 510(k) clearances

Decided510(k)Device and applicantCode
No clearances in this window.

Latest recalls

DateFirm and productCodeLinked 510(k)
Sep 2, 2025mo-Vis BVBA
IDM-ARLITE-R. Electrical wheelchair component.
Open, Classified
KNNNone listed
Sep 2, 2025mo-Vis BVBA
All-round Joystick R-net Light. Electrical wheelchair component.
Open, Classified
KNNNone listed
Sep 2, 2025mo-Vis BVBA
IDM-MULTI-R. Electrical wheelchair component.
Open, Classified
KNNNone listed
Sep 2, 2025mo-Vis BVBA
IDM-MICRO-R. Electrical wheelchair component.
Open, Classified
KNNNone listed
Sep 2, 2025mo-Vis BVBA
Multi Joystick R-net. Electrical wheelchair component.
Open, Classified
KNNNone listed
Sep 2, 2025mo-Vis BVBA
Micro Joystick R-net. Electrical wheelchair component.
Open, Classified
KNNNone listed
Jan 11, 2024mo-Vis BVBA
Scoot Control R-net, Product Number P015-61. The Scoot Control is intended to support a wheelchair attendant in controlling or maneuvering a power chair
Open, Classified
KNNNone listed
Get alerts for these product codes