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Tatum Surgical/Abutment (Post)

FDA UDI

Class II (US FDA UDI)

by Suncoast Dental, Inc.

Identity

Trade Name
Tatum Surgical/Abutment (Post) FDA UDI
Generic Name
Screw endosteal dental implant, two-piece FDA UDI
Device Name
Abutment/4.0mm x 60 degree Post Short FDA UDI
Model / Reference
Abutment/4.0mm x 60 degree Post Short FDA UDI
Description
Abutment/4.0mm x 60 degree Post Short FDA UDI

Identifiers

Catalog Number
PN40.60S FDA UDI
Primary DI / UDI-DI
00083208840609 FDA UDI
510(k) Number
K811923 FDA UDI
FDA Product Code
DZE FDA UDI
GMDN Term
Screw endosteal dental implant, two-piece FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3640 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

No

FDA UDI
MRI Safety
MR Safe FDA UDI

Dimensions & Sizes

Size
Angle — 60 degree FDA UDI
Height — 5 Millimeter FDA UDI
Outer Diameter — 4 Millimeter FDA UDI

Tatum Surgical/Abutment (Post) by Suncoast Dental, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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 7dc7fe4c-9790-4b29-8d82-76f84b5829fb 38 fields · synced May 31, 2026