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Inclusive

FDA UDI

Class II (US FDA UDI)

by Prismatik Dentalcraft, Inc.

Identity

Trade Name
Inclusive FDA UDI
Generic Name
Dental implant suprastructure, permanent, preformed FDA UDI
Device Name
Inclusive Titanium Abutment 4.5 mmH, Non-Engaging, compatible with: Dentsply Implants Astra Tech Implant System EV 3.6 FDA UDI
Model / Reference
70-1176-COM0221 FDA UDI
Description
Inclusive Titanium Abutment 4.5 mmH, Non-Engaging, compatible with: Dentsply Implants Astra Tech Implant System EV 3.6 FDA UDI

Identifiers

Catalog Number
70-1176-COM0221 FDA UDI
Primary DI / UDI-DI
D745701176COM02210 FDA UDI
510(k) Number
K191222 FDA UDI
FDA Product Code
NHA FDA UDI
GMDN Term
Dental implant suprastructure, permanent, preformed FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3630 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

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

Category: Dental implant suprastructure, permanent, preformed

Inclusive by Prismatik Dentalcraft, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental implant suprastructure, permanent, preformed.

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 51c608e9-8c82-4e5c-b720-cf2d450155b4 36 fields · synced May 31, 2026