4/5/6mm Crown & Bridge Driver

FDA UDI

Class I (US FDA UDI)

by Oco Biomedical

Identity

Trade Name: 4/5/6mm Crown & Bridge Driver FDA UDI
Generic Name: Surgical screwdriver, reusable FDA UDI
Device Name: 4/5/6mm C&B Driver (Short) Places 4/5mm ISI C&B Implants and 4/5mm Solid Abutments for TSI/ERI/Macro FDA UDI
Model / Reference: 4/5/6mm C&B Driver (Short) FDA UDI
Description: 4/5/6mm C&B Driver (Short) Places 4/5mm ISI C&B Implants and 4/5mm Solid Abutments for TSI/ERI/Macro FDA UDI

Identifiers

Catalog Number: 0075NS FDA UDI
Primary DI / UDI-DI: D7850075NS0 FDA UDI
FDA Product Code: NDP FDA UDI
GMDN Term: Surgical screwdriver, reusable FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 872.3980 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

Yes

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Surgical screwdriver, reusable

4/5/6mm Crown & Bridge Driver by Oco Biomedical — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical screwdriver, reusable.

Fortex Pedicle Screw System — Xtant Medical Holdings, Inc. · Class II
MEGA PLUS SPINE SYSTEM — BK MEDITECH CO., LTD. · Class I
Inclusive — PRISMATIK DENTALCRAFT, INC. · Class I
LOSPA IS Spinal Fixation System — Corentec Co., Ltd · Class II
PERLA ® TL — Spineart · Class II
USS — Synthes · Class I
Whistler Modular Pedicle Screw System — EVOLUTION SPINE, LLC · Class I
CosmoLock Pedicle Screw System — Kalitec Direct LLC · 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer: Oco Biomedical

Sources (1)

FDA UDI 191ae7c0-7081-41fb-8a77-133fb0c41265 34 fields · synced Jun 8, 2026