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Endo Access Bur

FDA UDI

Class I (US FDA UDI)

by Tulsa Dental Products Llc

Identity

Trade Name
Endo Access Bur FDA UDI
Generic Name
Diamond dental bur, single-use FDA UDI
Device Name
Endo Access Bur FG 2-4-6 FDA UDI
Model / Reference
A016430090020 FDA UDI
Description
Endo Access Bur FG 2-4-6 FDA UDI

Identifiers

Catalog Number
A016430090020 FDA UDI
Primary DI / UDI-DI
D7166688032 FDA UDI
FDA Product Code
DZP FDA UDI
GMDN Term
Diamond dental bur, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4535 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

Yes

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: Diamond dental bur, single-use

Endo Access Bur by Tulsa Dental Products Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Diamond dental bur, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Tulsa Dental Products Llc

Sources (1)

  • FDA UDI 44be36ae-245b-438b-9ca9-dbc53cd666df 34 fields · synced Jun 1, 2026