BOSS Instruments

FDA UDI

Class I (US FDA UDI)

by Boss Instruments, Ltd.

Identity

Trade Name: BOSS Instruments FDA UDI
Generic Name: Neurosurgical curette, reusable FDA UDI
Device Name: Spinal Fusion Cur, rnd knld hndl, str, oval, sz 000, 9" FDA UDI
Model / Reference: 70-7335 FDA UDI
Description: Spinal Fusion Cur, rnd knld hndl, str, oval, sz 000, 9" FDA UDI

Identifiers

Catalog Number: 70-7335 FDA UDI
Primary DI / UDI-DI: 00888515161955 FDA UDI
FDA Product Code: HAO FDA UDI
GMDN Term: Neurosurgical curette, reusable FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 882.4535 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Neurosurgical curette, reusable

BOSS Instruments by Boss Instruments, Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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OptiMesh Multiplanar Expandable Interbody Fusion System — SPINEOLOGY INC. · Class I
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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 I	Pending data

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Manufacturer

Manufacturer: Boss Instruments, Ltd.

Sources (1)

FDA UDI b45d2897-bca2-44e9-b89f-e2d2e7ee7b61 35 fields · synced Jun 9, 2026