OsteoCove

FDA UDI

Class II (US FDA UDI)

by SeaSpine Orthopedics Corporation

Identity

Trade Name: OsteoCove FDA UDI
Generic Name: Bone matrix implant, composite FDA UDI
Device Name: OsteoCove Strip, 10cc FDA UDI
Model / Reference: 56930100 FDA UDI
Description: OsteoCove Strip, 10cc FDA UDI

Identifiers

Catalog Number: 56930100 FDA UDI
Primary DI / UDI-DI: 10889981309077 FDA UDI
510(k) Number: K230486 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

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: Bone matrix implant, composite

OsteoCove by SeaSpine Orthopedics Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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MacroFORM Bioactive Packable Graft 5.0cc — NovaBone Products, LLC · Class II

Cleared under the same submission

K230486 also covers:

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: SeaSpine Orthopedics Corporation

Sources (1)

FDA UDI e041c48f-9019-4196-9c36-46764b6848b1 36 fields · synced Jun 8, 2026