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Tatum Serrated Offset Surgical Curette 10S

FDA UDI

Class I (US FDA UDI)

by Suncoast Dental, Inc.

Identity

Trade Name
Tatum Serrated Offset Surgical Curette 10S FDA UDI
Generic Name
Bone curette, reusable FDA UDI
Device Name
Serrated Offset double ended Surgical Curette 10S FDA UDI
Model / Reference
Serrated Offset Surgical Curette 10S FDA UDI
Description
Serrated Offset double ended Surgical Curette 10S FDA UDI

Identifiers

Catalog Number
Curette Off/Serrated 10S FDA UDI
Primary DI / UDI-DI
00083208131103 FDA UDI
FDA Product Code
FZS FDA UDI
GMDN Term
Bone curette, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

Yes

FDA UDI

Lot / Batch Number

Yes

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: Bone curette, reusable

Tatum Serrated Offset Surgical Curette 10S by Suncoast Dental, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone curette, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 5f68a6a7-8779-40fa-a7b8-927332f1341d 35 fields · synced May 30, 2026