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
Moist Heat or Steam Sterilization FDA UDI
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
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Also classified as Screw endosteal dental implant, two-piece.
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Cleared under the same submission
K131557 also covers:
- Ritter Dental Implant System — Ritter Implants GmbH CO KG
- Ritter Dental Implant System — Ritter Implants GmbH CO KG
- Ritter Dental Implant System — Ritter Implants GmbH CO KG
- Ritter Dental Implant System — Ritter Implants GmbH CO KG
- Ritter Dental Implant System — Ritter Implants GmbH CO KG
- Ritter Dental Implant System — Ritter Implants GmbH CO KG
- Ritter Dental Implant System — Ritter Implants GmbH CO KG
- Ritter Dental Implant System — Ritter Implants GmbH CO KG
- Ritter Dental Implant System — Ritter Implants GmbH CO KG
- Ritter Dental Implant System — Ritter Implants GmbH CO KG
- Ritter Dental Implant System — Ritter Implants GmbH CO KG
- Ritter Dental Implant System — Ritter Implants GmbH CO KG
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Ritter Implants GmbH CO KG
Sources (1)
- FDA UDI d00d310a-361f-4a56-8bd3-22ea8ecb986f 33 fields · synced May 30, 2026