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Prima

FDA UDI

Class I (US FDA UDI)

by Keystone Dental Inc.

Identity

Trade Name
Prima FDA UDI
Generic Name
Fixture/appliance dental drill bit, reusable FDA UDI
Device Name
Tissue Punch FDA UDI
Model / Reference
15671K FDA UDI
Description
Tissue Punch FDA UDI

Identifiers

Primary DI / UDI-DI
D76815671K0 FDA UDI
FDA Product Code
DZA FDA UDI
GMDN Term
Fixture/appliance dental drill bit, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4130 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

Category: Fixture/appliance dental drill bit, reusable

Prima by Keystone Dental Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Fixture/appliance dental drill bit, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 0ee4a2b7-bcc1-48f1-af4d-968e9fd60e81 34 fields · synced Jun 8, 2026