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Ritter Dental Implant System

FDA UDI

Class II (US FDA UDI)

by Ritter Implants GmbH CO KG

Identity

Trade Name
Ritter Dental Implant System FDA UDI
Generic Name
Screw endosteal dental implant, two-piece FDA UDI
Model / Reference
SLTA-9 FDA UDI

Identifiers

Primary DI / UDI-DI
ERITSLTA92 FDA UDI
510(k) Number
K131557 FDA UDI
FDA Product Code
NHA FDA UDI
GMDN Term
Screw endosteal dental implant, two-piece 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

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

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

Category: Screw endosteal dental implant, two-piece

Ritter Dental Implant System by Ritter Implants GmbH CO KG — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Screw endosteal dental implant, two-piece.

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 d00d310a-361f-4a56-8bd3-22ea8ecb986f 33 fields · synced May 30, 2026