← Back to catalogue

Paralleling Pin

FDA UDI

Class I (US FDA UDI)

by Oco Biomedical

Identity

Trade Name
Paralleling Pin FDA UDI
Generic Name
Dental implantation depth/angle gauge, reusable FDA UDI
Device Name
5mm Paralleling Pin 5mm Diameter FDA UDI
Model / Reference
5mm Paralleling Pin FDA UDI
Description
5mm Paralleling Pin 5mm Diameter FDA UDI

Identifiers

Catalog Number
ISI-P 5.0 FDA UDI
Primary DI / UDI-DI
D785ISIP50 FDA UDI
FDA Product Code
NDP FDA UDI
GMDN Term
Dental implantation depth/angle gauge, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3980 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

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: Dental implantation depth/angle gauge, reusable

Paralleling Pin by Oco Biomedical — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental implantation depth/angle gauge, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Oco Biomedical

Sources (1)

  • FDA UDI 07538777-9431-4144-b35c-13fe34eb432c 34 fields · synced May 30, 2026