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Perfect Finish

FDA UDI

Class I (US FDA UDI)

by Lares Research, Inc.

Identity

Trade Name
Perfect Finish FDA UDI
Generic Name
Dental surgical power tool motorized handpiece/set, pneumatic FDA UDI
Device Name
Perfect Finish 1:1 Straight Attachment FDA UDI
Model / Reference
1:1 Straight Attachment FDA UDI
Description
Perfect Finish 1:1 Straight Attachment FDA UDI

Identifiers

Catalog Number
11627 FDA UDI
Primary DI / UDI-DI
D950116270 FDA UDI
510(k) Number
K961163 FDA UDI
FDA Product Code
EFB FDA UDI
GMDN Term
Dental surgical power tool motorized handpiece/set, 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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dental surgical power tool motorized handpiece/set, pneumatic

Perfect Finish by Lares Research, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental surgical power tool motorized handpiece/set, pneumatic.

Cleared under the same submission

K961163 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Lares Research, Inc.

Sources (1)

  • FDA UDI 68649479-3007-409e-86fe-d18dedb14b86 36 fields · synced May 30, 2026