Bioactive Strip 10.0cc Long

FDA UDI

Class II (US FDA UDI)

by NovaBone Products, LLC

Identity

Trade Name: Bioactive Strip 10.0cc Long FDA UDI
Generic Name: Bone matrix implant, composite FDA UDI
Device Name: Synthetic bone void filler for orthopedic applications FDA UDI
Model / Reference: OX3010ST FDA UDI
Description: Synthetic bone void filler for orthopedic applications FDA UDI

Identifiers

Catalog Number: NB2310LOX FDA UDI
Primary DI / UDI-DI: 00813909013299 FDA UDI
FDA Product Code: MQV FDA UDI
GMDN Term: Bone matrix implant, composite FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 888.3045 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: Bone matrix implant, composite

Bioactive Strip 10.0cc Long by NovaBone Products, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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STRATOFUSE Strip — Berkeley Advanced Biomaterials · Class II
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AlexiFuse Synthetic Foam Strip — Berkeley Advanced Biomaterials · Class II
BiSyntek Putty — Berkeley Advanced Biomaterials · Class II
nanOss 3D Plus Advanced Bone Graft Substitute — Xtant Medical Holdings, Inc. · Class II

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: NovaBone Products, LLC

Sources (1)

FDA UDI b94e75dc-97f8-47ca-927a-5fe54130b7ec 36 fields · synced Jun 9, 2026