← Back to catalogue

TatumSurgical/Abutment (Post)

FDA UDI

Class II (US FDA UDI)

by Suncoast Dental, Inc.

Identity

Trade Name
TatumSurgical/Abutment (Post) FDA UDI
Generic Name
Screw endosteal dental implant, two-piece FDA UDI
Device Name
Implant Abutment 5.0mm x 50 degree -9mm Height FDA UDI
Model / Reference
Abutment/5.0mm x 50 degree Post FDA UDI
Description
Implant Abutment 5.0mm x 50 degree -9mm Height FDA UDI

Identifiers

Catalog Number
PN50.50 FDA UDI
Primary DI / UDI-DI
00083208750502 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
Height — 9 Millimeter FDA UDI
Angle — 50 degree FDA UDI
Outer Diameter — 5 Millimeter FDA UDI

TatumSurgical/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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 69bf54a0-c401-495f-b7b3-220c47ba9709 38 fields · synced May 31, 2026