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Tatum Surgical-Analog

FDA UDI

Class I (US FDA UDI)

by Suncoast Dental, Inc.

Identity

Trade Name
Tatum Surgical-Analog FDA UDI
Generic Name
Dental implant analog FDA UDI
Device Name
Dental Analog, ITO Unipost Crown and Bridge 3.5mm FDA UDI
Model / Reference
Analog (CB) 3.5 FDA UDI
Description
Dental Analog, ITO Unipost Crown and Bridge 3.5mm FDA UDI

Identifiers

Catalog Number
Analog (CB) 3.5 FDA UDI
Primary DI / UDI-DI
00083208103810 FDA UDI
510(k) Number
K811923 FDA UDI
FDA Product Code
NDP FDA UDI
GMDN Term
Dental implant analog FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3980 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 3.5 Millimeter FDA UDI

Category: Dental implant analog

Tatum Surgical-Analog by Suncoast Dental, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental implant analog.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 32a46d74-4546-42cb-921b-5e4adda04c81 37 fields · synced Jun 8, 2026