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Sphero Block

FDA UDI

Class II (US FDA UDI)

by PREAT Corporation

Identity

Trade Name
Sphero Block FDA UDI
Generic Name
Dental implant suprastructure, permanent, preformed FDA UDI
Device Name
Sphero Block Abutment Sterioss Flat-Top 3.8mm x 1mm (2.5mm Ball) FDA UDI
Model / Reference
0818652 FDA UDI
Description
Sphero Block Abutment Sterioss Flat-Top 3.8mm x 1mm (2.5mm Ball) FDA UDI

Identifiers

Catalog Number
0818652 FDA UDI
Primary DI / UDI-DI
00842092179901 FDA UDI
FDA Product Code
DZE FDA UDI
GMDN Term
Dental implant suprastructure, permanent, preformed FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3640 FDA UDI
Commercial Distribution
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

Yes

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

Category: Dental implant suprastructure, permanent, preformed

Sphero Block by PREAT Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental implant suprastructure, permanent, preformed.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
PREAT Corporation

Sources (1)

  • FDA UDI c8a718c9-f828-40a0-a044-60eb06271201 35 fields · synced Jun 8, 2026