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Axiobionics, LLC

Last updated May 23, 2026

Information

Country: US
Address: —
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DUNS Number: —

Catalogue (64)

Page 1 of 2

Device	Model / Reference	Registries	Class	Status
BioUnitard	2	FDA UDI	Class II	Active
BioGel Velcro Electrode	2	FDA UDI	Class II	Active
LE BioSleeve	0	FDA UDI	Class II	Active
BioGel Velcro Electrode	2	FDA UDI	Class II	Active
BioShorts	0	FDA UDI	Class II	Active
FreeStep	0	FDA UDI	Class II	Active
BioBrief	0	FDA UDI	Class II	Active
OOFS Pace XL Stimulator	0	FDA UDI	Class II	Active
UE BioSleeve	1	FDA UDI	Class II	Active
BioMiniVest	0	FDA UDI	Class II	Active
BioGel Velcro Electrode	2	FDA UDI	Class II	Active
BioBelt Ab	0	FDA UDI	Class II	Active
BioGel Velcro Electrode	2	FDA UDI	Class II	Active
BioGel Velcro Electrode	2	FDA UDI	Class II	Active
LE BioSleeve	0	FDA UDI	Class II	Active
BioGel Velcro Electrode	2	FDA UDI	Class II	Active
BioGel Velcro Electrode	2	FDA UDI	Class II	Active
BioGel Velcro Electrode	2	FDA UDI	Class II	Active
BioGel Velcro Electrode	2	FDA UDI	Class II	Active
BioCollar	3	FDA UDI	Class II	Unknown
BioBelt Ab Large Expanded	0	FDA UDI	Class II	Active
LE BioSleeve	7	FDA UDI	Class II	Unknown
Adhesive Electrode	0	FDA UDI	Class II	Active
LE BioSleeve	0	FDA UDI	Class II	Active
BioGel Velcro Electrode	2	FDA UDI	Class II	Active
BioGel Velcro Electrode	2	FDA UDI	Class II	Active
UE BioSleeve	5	FDA UDI	Class II	Active
Axio 2 Channel Stimulator	0	FDA UDI	Class II	Active
EMPI Focus 2 Channel Stimulator	0	FDA UDI	Class II	Active
BioGel Velcro Electrode	2	FDA UDI	Class II	Active
Spectra 360 Electrode Gel	0	FDA UDI	Class II	Active
LE BioSleeve	1	FDA UDI	Class II	Active
UE BioSleeve	4	FDA UDI	Class II	Active
Axio 4 Channel Stimulator	0	FDA UDI	Class II	Active
EMPI Continuum	0	FDA UDI	Class II	Active
BioGel Velcro Electrode	2	FDA UDI	Class II	Active
UE BioSleeve	0	FDA UDI	Class II	Active
BioShortX	1	FDA UDI	Class II	Active
UE BioSleeve	0	FDA UDI	Class II	Active
UE BioSleeve	0	FDA UDI	Class II	Active
NeuroPro 4 NMES Stimulator	0	FDA UDI	Class II	Active
BioMiniBelt	4	FDA UDI	Class II	Active
BioBelt Lumbar Contoured	1	FDA UDI	Class II	Active
UE BioSleeve	4	FDA UDI	Class II	Active
BioGel Velcro Electrode	2	FDA UDI	Class II	Active
LE BioSleeve	1	FDA UDI	Class II	Active
UE BioSleeve	4	FDA UDI	Class II	Active
LE BioSleeve	0	FDA UDI	Class II	Active
BioCollar	4	FDA UDI	Class II	Active
BioVest	1	FDA UDI	Class II	Active

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FDA Recalls (4)

Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.

Date	Recall No.	Class	Status	Reason
May 27, 2011	Z-2899-2011	—	terminated	Premature Device Failure : Failure of the electrode sites to conduct and provide muscle stimulation due to silver fabric component failure.
May 27, 2011	Z-2898-2011	—	terminated	Premature Device Failure : Failure of the electrode sites to conduct and provide muscle stimulation due to silver fabric component failure.
May 27, 2011	Z-2900-2011	—	terminated	Premature Device Failure : Failure of the electrode sites to conduct and provide muscle stimulation due to silver fabric component failure.
May 27, 2011	Z-2901-2011	—	terminated	Premature Device Failure : Failure of the electrode sites to conduct and provide muscle stimulation due to silver fabric component failure.