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Scott's Select Cleoid-Discoid De # 89-92

FDA UDI

Class I (US FDA UDI)

by Scott's Dental Supply L.l.c.

Identity

Trade Name
SCOTT'S SELECT CLEOID-DISCOID DE # 89-92 FDA UDI
Generic Name
Dental restoration carver, multiple-material FDA UDI
Device Name
CARVER (1/pack) End: Double End, Size: CD 89-92, Handle: Standard; For more information: https://www.scottsdental.com/catalog/product/view/id/29892/s/carvers-scott-s-select/ FDA UDI
Model / Reference
128-1591 FDA UDI
Description
CARVER (1/pack) End: Double End, Size: CD 89-92, Handle: Standard; For more information: https://www.scottsdental.com/catalog/product/view/id/29892/s/carvers-scott-s-select/ FDA UDI

Identifiers

Catalog Number
128-1591 FDA UDI
Primary DI / UDI-DI
D77812815910 FDA UDI
FDA Product Code
EKH FDA UDI
GMDN Term
Dental restoration carver, multiple-material FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4565 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

No

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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dental restoration carver, multiple-material

Scott's Select Cleoid-Discoid De # 89-92 by Scott's Dental Supply L.l.c. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental restoration carver, multiple-material.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI cb97c571-8e7b-4107-b2dc-28f227e553d8 35 fields · synced Jun 1, 2026