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Misonix, LLC

Last updated September 17, 2026

About

Bioventus products, orthobiologics, biologics and devices for bone healing and osteoartritis pain relief are known as innovations for active healing.

From the manufacturer's own website. Source

Information

Country: US
Address: 1938 New Hwy, Farmingdale, NY, 11735
Website: www.bioventus.com
LinkedIn: linkedin.com/company/bioventus
Facebook: —
Email: —
Phone: —
PRRC Contact: —
EUDAMED SRN: —
FDA FEI Number: 2435119
DUNS Number: —

Catalogue (204)

Page 2 of 5

Device	Model / Reference	Registries	Class	Status
neXus	140-33-4420	FDA UDI	U	Active
SonicOne Clinic	E-SOP-R2	FDA UDI	U	Active
SonaStar	CFSM5-T101	FDA UDI	Class II	Active
neXus	140-35-1426	FDA UDI	U	Active
BoneScalpel	BCM-FS	FDA UDI	U	Active
neXus	110-31-1220	FDA UDI	U	Active
neXus	100-24-0003	FDA UDI	U	Active
neXus	110-31-1230	FDA UDI	U	Active
neXus	100-50-0000	FDA UDI	U	Active
neXus	100-24-0001	FDA UDI	U	Active
neXus	100-60-0000	FDA UDI	U	Active
BoneScalpel	MXB-B1	FDA UDI	U	Active
SonaStar	SYSTEM-M260-0 (Rev L or higher)	FDA UDI	Class II	Active
SonaStar	CFSM6-C140	FDA UDI	U	Active
BoneScalpel	MXB-10LC	FDA UDI	U	Active
SonaStar	MXA-D230	FDA UDI	Class II	Active
neXus	110-31-1210	FDA UDI	U	Active
SonaStar	MXA-D226	FDA UDI	Class II	Active
SonaStar	MXA-D232	FDA UDI	Class II	Active
neXus	130-35-1220	FDA UDI	U	Active
neXus	110-31-2120	FDA UDI	U	Active
BoneScalpel	MXB-20	FDA UDI	U	Active
neXus	100-25-0002	FDA UDI	U	Active
SonaStar	SYSTEM-M260-2 (Rev Kx)	FDA UDI	U	Active
SonaStar	SYSTEM-M380-1	FDA UDI	Class II	Active
neXus	100-29-0000	FDA UDI	U	Active
neXus	100-10-0002	FDA UDI	Class II	Active
SonaStar	SYSTEM-M260-2(Rev L or higher)	FDA UDI	Class II	Active
BoneScalpel & SonicOne (O.R.)	E-SYSTRAY	FDA UDI	U	Active
SonaStar	CFSX6-H322	FDA UDI	Class II	Active
SonicOne Clinic	E-SOP-GEN	FDA UDI	U	Active
SonaStar	CFSM6-C142	FDA UDI	U	Active
SonaStar	SYSTEM-M360-2	FDA UDI	Class II	Active
neXus	110-31-2110	FDA UDI	U	Active
SonaStar	SYSTEM-M200-3	FDA UDI	Class II	Active
SonaStar	SYSTEM-M280-3 (rev Jx)	FDA UDI	Class II	Active
BoneScalpel	MXB-MIS-S1	FDA UDI	U	Active
neXus	110-31-5501	FDA UDI	U	Active
SonicOne Clinic	E-SOP-HP	FDA UDI	U	Active
SonicOne O.R.	MXC-X2	FDA UDI	U	Active
neXus	100-61-0000	FDA UDI	U	Active
SonaStar	MXA-D214	FDA UDI	Class II	Active
neXus	130-35-1416	FDA UDI	U	Active
BoneScalpel	MXB-T	FDA UDI	U	Active
SonaStar	CFSM6-T222	FDA UDI	Class II	Active
SonicOne O.R.	E-SOC-FTHH	FDA UDI	U	Active
SonicOne O.R.	MXC-SHAVER-360	FDA UDI	U	Active
SonaStar	CFSM6-H175	FDA UDI	Class II	Active
neXus	100-21-0000	FDA UDI	U	Active
neXus	100-10-0000	FDA UDI	Class II	Active

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FDA Recalls (1)

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
Aug 13, 2003	Z-0070-04	—	terminated	Firm received complaints of tingling or static shock sensation to end users caused by forcing the output connector into its receptacle misaligned. The misalignment causes additional voltage to appear on the patient probe.