← Back to catalogue

Neodent Implant System

FDA UDI

Class II (US FDA UDI)

by Institut Straumann SA

Identity

Trade Name
Neodent Implant System FDA UDI
Generic Name
Dental bridge, polymer FDA UDI
Device Name
Screw-retained Bridge, Full-arch, PMMA FDA UDI
Model / Reference
Bridges (tooth borne) FDA UDI
Description
Screw-retained Bridge, Full-arch, PMMA FDA UDI

Identifiers

Catalog Number
010.0304 FDA UDI
Primary DI / UDI-DI
07630031779977 FDA UDI
FDA Product Code
NHA FDA UDI
GMDN Term
Dental bridge, polymer FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3630 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

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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Dental bridge, polymer

Neodent Implant System by Institut Straumann SA — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental bridge, polymer.

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
Institut Straumann SA

Sources (1)

  • FDA UDI 1f9eda07-14e8-4390-b1f4-04a72a7e912f 35 fields · synced Jun 8, 2026