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Sign in to claim this brandRHEIN 83 SRL
US
Last updated May 23, 2026
What RHEIN 83 SRL makes
Rhein 83 SRL manufactures dental implant suprastructures, including preformed permanent frameworks for crowns and bridges, as well as reusable dental implant holding endpieces. The company also produces preformed root canal posts, designed for internal dental reinforcement. Titanium and other materials are used in these components to ensure compatibility with dental implants.
The portfolio includes devices classified as Class I and Class II under FDA regulations, all of which are listed in the FDA’s Unique Device Identification (UDI) system. The company is based in the United States.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What types of medical devices does Rhein 83 SRL manufacture?
Rhein 83 SRL specializes in dental devices, primarily producing dental implant suprastructures like preformed permanent frameworks for crowns and bridges. They also make reusable dental implant holding endpieces and preformed root canal posts, which are used for reinforcing teeth internally. These devices are designed to integrate with dental implants and are crafted from materials like titanium to ensure compatibility.
Where is Rhein 83 SRL based?
Rhein 83 SRL is based in the United States. The company’s headquarters and operations are located within this country, though specific regional offices or manufacturing sites may vary.
Which regulatory registries list Rhein 83 SRL’s devices?
Rhein 83 SRL’s devices are listed in the FDA’s Unique Device Identification (UDI) system. This registry ensures traceability and transparency for dental implant suprastructures, holding endpieces, and root canal posts, which fall under Class I and Class II classifications.
How are Rhein 83 SRL’s devices classified under FDA regulations?
Rhein 83 SRL’s devices are classified as either Class I or Class II under FDA regulations. Class I devices generally pose minimal risk and require less regulatory oversight, while Class II devices involve a moderate risk and require special controls to ensure safety and effectiveness. The classification depends on factors like the device’s intended use and potential health impact.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
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- Website
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- Phone
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- PRRC Contact
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- EUDAMED SRN
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- FDA FEI Number
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- DUNS Number
- 439240722
Catalogue (4428)
Page 89 of 89| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Ot Equator Titanium Abutment | OT EQUATOR CERTAIN 3i DIAMETER 6 H 6 | FDA UDI | Class II | Active |
| Ot Equator Titanium Abutment | ASTRA TECH LILAC H 1 | FDA UDI | Class II | Active |
| Ot Equator Titanium Abutment | OT EQUATOR MIS - SEVEN ø 3,75-4,2 h.0,5 | FDA UDI | Class II | Active |
| Ot Equator Titanium Abutment | CERTAIN 3i DIAMETER 4,1 H 0,5 | FDA UDI | Class II | Unknown |
| Dental Attachments | EQUATOR THREADED SLEEVE SYSTEM x BONDING | FDA UDI | Class I | Active |
| Direct Titanium Attachments | OT CAP IMPRESSION COPINGS MICRO SIZE 2 p | FDA UDI | Class I | Unknown |
| Ot Equator Titanium Abutment | OT EQUATOR STRAUMANN RN H 4 | FDA UDI | Class II | Unknown |
| Ot Equator Titanium Abutment | SCREW VENT DIAMETER 5,7 H 3 | FDA UDI | Class II | Active |
| Invasive Accessories And Instruments | BROKEN SCREW EXT.KIT ZIMMER ø 3,75 - 4,5 | FDA UDI | Class I | Unknown |
| Ot Equator Titanium Abutment | OT EQUATOR BIO HORIZONS ø 3,5 h.3 TiN | FDA UDI | Class II | Active |
| Dental Attachments | OT CAP TECNO NORMO | FDA UDI | Class I | Unknown |
| Dental Attachments | GREY CAPS STANDARD size x6 | FDA UDI | Class I | Active |
| Ot Equator Titanium Abutment | OT EQUATOR CERTAIN ø 5 h.0,5 | FDA UDI | Class II | Active |
| Ot Equator Titanium Abutment | OT EQUATOR IP Piccolo H/E ø 3 h.2 | FDA UDI | Class II | Active |
| Ot Equator Titanium Abutment | OT EQUATOR SWISS PLUSS OCTAGONAL H 0,5 | FDA UDI | Class II | Active |
| Ot Equator Titanium Abutment | STRAUMANN WN H 3 | FDA UDI | Class II | Active |
| Ot Equator Titanium Abutment | CERTAIN 3i DIAMETER 4,1 H 3 | FDA UDI | Class II | Unknown |
| Endodontic Posts | PIVOT FLEX mm.10,2 RIV.TiN | FDA UDI | Class I | Active |
| Dental Equipments | IMPRESSION COPINGS 100 u. | FDA UDI | Class I | Unknown |
| Ot Equator Titanium Abutment | ASTRA TECH AQUA H 4 | FDA UDI | Class II | Unknown |
| Ot Equator Titanium Abutment | OT EQUATOR ASTRA EV ø 4,2 h.5 | FDA UDI | Class II | Unknown |
| Ot Equator Titanium Abutment | OT EQUATOR BONE LEVEL NC H 4 | FDA UDI | Class II | Active |
| Ot Equator Titanium Abutment | STRAUMANN WN H 1 | FDA UDI | Class II | Active |
| Dental Attachments | RESILIENT CAPS NORMAL S.gold colour pz.6 | FDA UDI | Class I | Unknown |
| Invasive Accessories And Instruments | MOOSER BUR FOR PIVOTS mms.7-9-10 mm | FDA UDI | Class I | Active |
| Dental Attachments | BALL ABUT. EXTRA SOFT CAP 500g YELLOW #4 | FDA UDI | Class I | Active |
| Ot Equator Titanium Abutment | BRANEMARK NP H 4 | FDA UDI | Class II | Active |
| Modification Of: Sphero Flex, Pivot Flex, And Sphero Block | K033630 | FDA 510(k) | Class II | Active |
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FDA Establishments (1)
Establishments registered with the FDA under this company group, matched by name.
- Rhein 83 Srl BOLOGNA Emilia-Romagna · IT FEI 3002807996