← Back to catalogue

SMARTmatic PROPHY S31

FDA UDI

Class I (US FDA UDI)

by KaVo Dental GmbH

Identity

Trade Name
SMARTmatic PROPHY S31 FDA UDI
Generic Name
Dental surgical power tool motor, electric FDA UDI
Device Name
This is a medical device. FDA UDI
Model / Reference
1.011.6760 FDA UDI
Description
This is a medical device. FDA UDI

Identifiers

Catalog Number
S31 FDA UDI
Primary DI / UDI-DI
EKAV101167600 FDA UDI
510(k) Number
K163239 FDA UDI
FDA Product Code
EFA FDA UDI
GMDN Term
Dental surgical power tool motor, electric 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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dental surgical power tool motor, electric

SMARTmatic PROPHY S31 by KaVo Dental GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental surgical power tool motor, electric.

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

Manufacturer
KaVo Dental GmbH

Sources (1)

  • FDA UDI 68bbd183-a909-4274-bdec-fbff5e0457f5 37 fields · synced Jun 1, 2026