Novo Surgical

FDA UDI

Class I (US FDA UDI)

by Novo Surgical, Inc.

Identity

Trade Name: Novo Surgical FDA UDI
Generic Name: Bone-coring punch, reusable FDA UDI
Device Name: bi-color ceramic cut micro kerrison detachable rongeur, 40 degrees up, small handles, 9.0 mm opening, black/gold titanium nitride coat, thin footplate, 1.0 mm bite, 7" (17.8 cm) FDA UDI
Model / Reference: N6922-91CG FDA UDI
Description: bi-color ceramic cut micro kerrison detachable rongeur, 40 degrees up, small handles, 9.0 mm opening, black/gold titanium nitride coat, thin footplate, 1.0 mm bite, 7" (17.8 cm) FDA UDI

Identifiers

Catalog Number: N6922-91CG FDA UDI
Primary DI / UDI-DI: G586N692291CG0 FDA UDI
FDA Product Code: HTX FDA UDI
GMDN Term: Bone-coring punch, reusable FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 888.4540 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: Bone-coring punch, reusable

Novo Surgical by Novo Surgical, Inc. — 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: Novo Surgical, Inc.

Sources (1)

FDA UDI 30ec37fd-1105-4e74-9875-0ce6db2735cf 35 fields · synced Jun 6, 2026