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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
NC/RC SRBB Bone Level screw, 025.2926 FDA UDI
Model / Reference
Screws FDA UDI
Description
NC/RC SRBB Bone Level screw, 025.2926 FDA UDI

Identifiers

Catalog Number
010.1100 FDA UDI
Primary DI / UDI-DI
07630031702326 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
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
MRI Safety
MR Conditional FDA UDI

Category: Dental implant suprastructure, permanent, preformed

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

Similar devices

Also classified as Dental implant suprastructure, permanent, preformed.

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 40fe8a48-b1f0-44b6-8f4e-8c8f0894c73c 35 fields · synced Jun 6, 2026