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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 3 of 5

Device	Model / Reference	Registries	Class	Status
SonaStar	MXA-PA	FDA UDI	Class II	Active
SonaStar	SYSTEM-M200-2	FDA UDI	U	Active
SonaStar	SYSTEM-M260-3 (rev Kx)	FDA UDI	Class II	Active
SonaStar	SYSTEM-M200-1	FDA UDI	Class II	Active
neXus	130-33-3419	FDA UDI	U	Active
SonaStar	MXA-L002	FDA UDI	Class II	Active
neXus	130-33-2210	FDA UDI	U	Active
SonicOne O.R.	MXC-X2-VAC	FDA UDI	U	Active
SonicOne Clinic	E-IRRTUBE9	FDA UDI	U	Active
SonaStar	MXA-D228	FDA UDI	Class II	Active
neXus	110-31-1120	FDA UDI	U	Active
BoneScalpel	MXB-S1	FDA UDI	U	Active
neXus	110-31-1110	FDA UDI	U	Active
BoneScalpel	MXB-S2	FDA UDI	U	Active
SonaStar	SYSTEM-M380-2	FDA UDI	Class II	Active
neXus	100-70-0000	FDA UDI	U	Active
neXus	120-31-13X2	FDA UDI	U	Active
SonaStar	CFSX6-H222 (Rev Hx)	FDA UDI	Class II	Active
SonaStar	CFSX6-H321	FDA UDI	Class II	Active
SonaStar	MXA-D218+	FDA UDI	Class II	Active
neXus	100-25-0003	FDA UDI	U	Active
SonicOne O.R.	MXC-BLADE-XL	FDA UDI	U	Active
SonaStar	SYSTEM-M200-0 (rev Ax)	FDA UDI	Class II	Active
neXus	100-71-0000	FDA UDI	U	Active
SonicOne O.R	MXC-BLADE-L	FDA UDI	U	Active
neXus	100-24-0004	FDA UDI	U	Active
SonaStar	CFSM5-C136	FDA UDI	Class II	Active
SonicOne (O.R. & Clinic)	E-GPC	FDA UDI	U	Active
neXus	120-31-10R1	FDA UDI	U	Active
SonaStar	SYSTEM-M260-3 (Rev L or higher)	FDA UDI	Class II	Active
SonicOne O.R.	MXC-BLADE-LS	FDA UDI	U	Active
BoneScalpel	MXB-S3	FDA UDI	U	Active
BoneScalpel	BCM-HP	FDA UDI	U	Active
SonaStar	CFSM6-H183	FDA UDI	Class II	Active
neXus	110-31-1125	FDA UDI	U	Active
SonaStar	MXA-D216	FDA UDI	Class II	Active
SonaStar	SYSTEM-M260-1 (Rev Kx)	FDA UDI	Class II	Active
neXus	130-33-2416	FDA UDI	U	Active
SonicOne O.R.	MXC-T	FDA UDI	U	Active
neXus	120-31-13C2	FDA UDI	U	Active
SonaStar	CFSX3-M200-1	FDA UDI	Class II	Active
SonicOne Clinic	E-SOP-X1	FDA UDI	U	Active
SonicOne O.R.	MXC-BLADE-LLC	FDA UDI	U	Active
SonicOne O.R.	MXC-X1	FDA UDI	U	Active
SonicOne (O.R. & Clinic)	E-PWRCH	FDA UDI	U	Active
BoneScalpel	BCM-CW	FDA UDI	U	Active
SonicOne OR	SOM-HP	FDA UDI	U	Active
BoneScalpel	BCM-GN	FDA UDI	U	Active
neXus	100-21-0001	FDA UDI	U	Active
BoneScalpel & SonicOne (O.R.)	BCM-2W	FDA UDI	U	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.