BOSS Instruments

FDA UDI

Class I (US FDA UDI)

by Boss Instruments, Ltd.

Identity

Trade Name: BOSS Instruments FDA UDI
Generic Name: Plastic surgery osteotome FDA UDI
Device Name: Boss Spinal Fusion Osteotome, str, 10mm, 9 1/2" FDA UDI
Model / Reference: 70-3950 FDA UDI
Description: Boss Spinal Fusion Osteotome, str, 10mm, 9 1/2" FDA UDI

Identifiers

Catalog Number: 70-3950 FDA UDI
Primary DI / UDI-DI: 00888515156203 FDA UDI
FDA Product Code: GFI FDA UDI
GMDN Term: Plastic surgery osteotome FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 878.4800 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: Plastic surgery osteotome

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

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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 6d6ebd4e-1f95-4c9f-b4ee-e1ebe0d6bfc3 35 fields · synced Jun 9, 2026