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Pathfinder Nxt Minimally Invasive Pedicle Screw System

FDA UDI

Class I (US FDA UDI)

by Institut Straumann SA

Identity

Trade Name
PATHFINDER NXT MINIMALLY INVASIVE PEDICLE SCREW SYSTEM FDA UDI
Generic Name
Dental implant suprastructure, permanent, preformed FDA UDI
Device Name
Basic Fixed Bar, 7 Implants, ZrO2/TAN FDA UDI
Model / Reference
Bridges (implant borne) FDA UDI
Description
Basic Fixed Bar, 7 Implants, ZrO2/TAN FDA UDI

Identifiers

Catalog Number
010.7095 FDA UDI
Primary DI / UDI-DI
07630031704764 FDA UDI
FDA Product Code
EHO FDA UDI
GMDN Term
Dental implant suprastructure, permanent, preformed FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3165 FDA UDI
Commercial Distribution
Not 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

No

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

Pathfinder Nxt Minimally Invasive Pedicle Screw System by Institut Straumann SA — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Institut Straumann SA

Sources (1)

  • FDA UDI c0b4a8a9-95a7-4162-a37a-120021917287 36 fields · synced Jun 8, 2026