← Back to catalogue

Lynx 4:1 Reduction Contra Angle

FDA UDI

Class I (US FDA UDI)

by Mti Precision Products

Identity

Trade Name
LYNX 4:1 REDUCTION CONTRA ANGLE FDA UDI
Generic Name
Dental power tool handpiece motorless component FDA UDI
Device Name
LYNX REDUCTION CONTRA ANGLE IS A LOWSPEED DENTAL HANDPIECE ATTACHMENT WHICH ACCEPTS DIFFERENT STYLES OF LATCH HEADS, PROPHY HEADS,SPRING AND FRICTION GRIP. WHICH WORK TOGETHER WITH AN E-TYPE MOTOR AS A 4:1 TRANSMISSION FROM THE MOTOR TO THE HEAD INCREASING THE TORQUE AND SLOWING THE MOTOR DOWN TO 1/4 IT'S SPEED. IT IS USED FOR THE POLISHING OF TEETH AND REMOVAL OF CARRIES IN A DENTAL SETTING. FDA UDI
Model / Reference
LX101 FDA UDI
Description
LYNX REDUCTION CONTRA ANGLE IS A LOWSPEED DENTAL HANDPIECE ATTACHMENT WHICH ACCEPTS DIFFERENT STYLES OF LATCH HEADS, PROPHY HEADS,SPRING AND FRICTION GRIP. WHICH WORK TOGETHER WITH AN E-TYPE MOTOR AS A 4:1 TRANSMISSION FROM THE MOTOR TO THE HEAD INCREASING THE TORQUE AND SLOWING THE MOTOR DOWN TO 1/4 IT'S SPEED. IT IS USED FOR THE POLISHING OF TEETH AND REMOVAL OF CARRIES IN A DENTAL SETTING. FDA UDI

Identifiers

Primary DI / UDI-DI
D826LX10104 FDA UDI
510(k) Number
K940261 FDA UDI
FDA Product Code
EGS FDA UDI
GMDN Term
Dental power tool handpiece motorless component 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 power tool handpiece motorless component

Lynx 4:1 Reduction Contra Angle by Mti Precision Products — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental power tool handpiece motorless component.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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

Manufacturer

Sources (1)

  • FDA UDI d4c62cf8-64fc-42f2-a0e8-f97508c8c2fa 34 fields · synced May 30, 2026