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Park Dental Research Corp.

FDA UDI

Class II (US FDA UDI)

by Park Dental Research Corp

Identity

Trade Name
Park Dental Research Corp. FDA UDI
Generic Name
Bone cutter FDA UDI
Device Name
NRpiezo + LED Narrow Ridge Piezo Surgical Unit w/LED FDA UDI
Model / Reference
D2-II FDA UDI
Description
NRpiezo + LED Narrow Ridge Piezo Surgical Unit w/LED FDA UDI

Identifiers

Catalog Number
NRP-1 FDA UDI
Primary DI / UDI-DI
D769NRP10 FDA UDI
510(k) Number
K111290 FDA UDI
FDA Product Code
DZI FDA UDI
GMDN Term
Bone cutter FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.4120 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

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Bone cutter

Park Dental Research Corp. by Park Dental Research Corp — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone cutter.

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 747e7335-1662-4557-a9bf-26161c5a0809 36 fields · synced May 30, 2026