Buxton BioMedical

FDA UDI

Class I (US FDA UDI)

by Buxton Biomedical, Inc.

Identity

Trade Name: Buxton BioMedical FDA UDI
Generic Name: Bone curette, reusable FDA UDI
Device Name: Spinal Fusion Curette,str.,00 FDA UDI
Model / Reference: 76-1162 FDA UDI
Description: Spinal Fusion Curette,str.,00 FDA UDI

Identifiers

Catalog Number: 76-1162 FDA UDI
Primary DI / UDI-DI: B7687611620 FDA UDI
FDA Product Code: FZS FDA UDI
GMDN Term: Bone curette, reusable 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

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

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Bone curette, reusable

Buxton BioMedical by Buxton Biomedical, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Novo Surgical — NOVO SURGICAL, INC. · Class I
Medicon — Medicon eG. Chirurgiemechaniker-Genossenschaft · Class I
Volkmann Bone Curette Oval - Fig. 00 17 cm - 6 3/4" Scoop Size 4.4 mm Stainless Steel — SURTEX INSTRUMENTS LTD · Class I

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: Buxton Biomedical, Inc.

Sources (1)

FDA UDI c2a25f55-a5bd-46ca-b7e8-0edeaf2671e2 34 fields · synced May 31, 2026