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Master Pro 5

FDA UDI

Class I (US FDA UDI)

by Mti Precision Products

Identity

Trade Name
MASTER PRO 5 FDA UDI
Generic Name
Dental surgical power tool motor, pneumatic FDA UDI
Device Name
MASTER PRO 5 A QUICK DISCONNECT 5000 RPM DENTAL MOTOR WITH PREMIUM LUBE FREE BEARINGS THAT ACCEPTS BURS, MANDRILS, DISCS, AND OTHER DRILL BITS TO PERFORM DRILLING AND POLISHING OF TEETH IN A DENTAL SETTING. FDA UDI
Model / Reference
50163-04 FDA UDI
Description
MASTER PRO 5 A QUICK DISCONNECT 5000 RPM DENTAL MOTOR WITH PREMIUM LUBE FREE BEARINGS THAT ACCEPTS BURS, MANDRILS, DISCS, AND OTHER DRILL BITS TO PERFORM DRILLING AND POLISHING OF TEETH IN A DENTAL SETTING. FDA UDI

Identifiers

Primary DI / UDI-DI
D8265016304 FDA UDI
510(k) Number
K070001 FDA UDI
FDA Product Code
EFB FDA UDI
GMDN Term
Dental surgical power tool motor, pneumatic FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4200 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dental surgical power tool motor, pneumatic

Master Pro 5 by Mti Precision Products — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental surgical power tool motor, pneumatic.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI bb7c0832-a521-46d6-a385-9ee7be6f413b 34 fields · synced Jun 8, 2026