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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 66 of 89| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Sphero Block Micro | S/BLOCK M ASTRA EV ø 3,6 h.5 | FDA UDI | Class II | Active |
| Sphero Block Normo | S/BLOCK NORMO LEGACY ø 3 h.3 TiN | FDA UDI | Class II | Unknown |
| Sphero Block Micro | SPHERO BLOCK Micro CORE VENT h.5 RIV.TiN | FDA UDI | Class II | Unknown |
| Ot Equator Titanium Abutment | BRANEMARK WP DIAMETER 5 H 6 | FDA UDI | Class II | Unknown |
| Ot Equator Titanium Abutment | BRANEMARK WP DIAMETER 6 H 4 | FDA UDI | Class II | Unknown |
| Sphero Flex | SPHERO FLEX REPLACE SELECT ø 5 h.2 TiN | FDA UDI | Class II | Active |
| Dental Equipments | PURPLE OT EQUATOR CAP 100 u. | FDA UDI | Class I | Unknown |
| Sphero Flex | SPHERO FLEX SPLINE ø 3,25 h.2 TiN | FDA UDI | Class II | Unknown |
| Direct Titanium Attachments | SPHERO BLOCK ANKYLOS C/X h.3 | FDA UDI | Class II | Unknown |
| Sphero Block Normo | S/BLOCK NORMO INTEGRAL ø 4 h.2 TiN | FDA UDI | Class II | Unknown |
| Sphero Flex | S/FLEX NOBEL ACTIVE NP ø 3,5 h.3 TiN | FDA UDI | Class II | Active |
| Sphero Block Normo | SET S.BLOCK N. IBS MAGICORE ø 4 h05 | FDA UDI | Class II | Active |
| Sphero Block Normo | S/BLOCK M. BONE LEVEL SC ø 2,9 h.6 TiN | FDA UDI | Class II | Active |
| Dental Equipments | YELLOW CAPS STANDARD size 500u. | FDA UDI | Class I | Unknown |
| Sphero Block Micro | S/BLOCK MICRO SPLINE ø 3,75-4 h.1,6 TiN | FDA UDI | Class I | Unknown |
| Ot Equator Titanium Abutment | MONC EQUATOR BIOHORIZONS ø4,5 h0,5 VER | FDA UDI | Class II | Active |
| Ot Equator-Ot Bridge | OT EQUATOR BONE LEVEL RC ø 4,1-4,8 h.4 | FDA UDI | Class I | Unknown |
| Ot Equator-Ot Bridge | OT EQUATOR ASTRA ST ø 4 h.6 | FDA UDI | Class I | Unknown |
| Ot Equator Titanium Abutment | OT EQUATOR ASTRA EV ø 3 h.3 | FDA UDI | Class II | Active |
| Ot Equator - Ot Bridge | OT EQUATOR SCREW VENT ø 5,7 h.4 | FDA UDI | Class II | Active |
| Sphero Block Micro | S/BLOCK M ENDOPORE E/Int.ø 5 h.4 TiN | FDA UDI | Class II | Unknown |
| Dental Equipments | GREEN CAP STANDARD SIZE 500u. | FDA UDI | Class I | Active |
| Sphero Block Normo | SPHERO BLOCK ANYRIDGE h.3 TiN | FDA UDI | Class II | Unknown |
| Ot Equator-Ot Bridge | OT EQUATOR TSII-GSII Mini ø 3,5 h.2 | FDA UDI | Class I | Unknown |
| Sphero Block Normo | S/BLOCK N ASTRA ACQUA ø3,5-4 h.7 TiN | FDA UDI | Class II | Unknown |
| OT Equator | Set OT Equator PREMIUM KHONO ø 3,3 + Smartbox h.2 | FDA UDI | Class II | Active |
| Sphero Block Normo | S/BLOCK N ASTRA ST ø 4 h.2 TiN | FDA UDI | Class II | Unknown |
| OT Equator | Set OT Equator NEOSS ø 3,25 + Smartbox h.2 | FDA UDI | Class II | Active |
| Sphero Block Normo | S/BLOCK N NOBEL ACTIVE ø 3 h.5 TiN | FDA UDI | Class II | Active |
| Ot Equator Titanium Abutment | CERTAIN 3i DIAMETER 3,25 H 2 | FDA UDI | Class II | Active |
| Sphero Block Normo | S/BLOCK N BONE LEVEL RC ø4,1-4,8 h.7 TiN | FDA UDI | Class II | Active |
| Ot Equator Titanium Abutment | FRIALIT XIVE DIAMETER 6,5 H 7 | FDA UDI | Class II | Unknown |
| Sphero Block Normo | S/BLOCK N ASTRA ST ø 4 h.1 TiN | FDA UDI | Class II | Unknown |
| Sphero Block Normo | S/BLOCK N BIO HORIZONS ø 3 h.5 TiN | FDA UDI | Class II | Active |
| Ot Equator-Ot Bridge | OT EQUATOR Frialit 2 ø 3 h.4 | FDA UDI | Class I | Unknown |
| Ot Equator-Ot Bridge | OT EQUATOR ANYRIDGE h.2 | FDA UDI | Class I | Unknown |
| Dental Equipments | CLEAR CAPS STANDARD size 50u. | FDA UDI | Class I | Active |
| Sphero Block Micro | SPHERO BLOCK MICRO ASTRA EV ø 3 h.4 Tin | FDA UDI | Class II | Active |
| Ot Equator - Ot Bridge | OT EQUATOR ReplaceSelect ø 4,3 h.2 | FDA UDI | Class II | Active |
| Dental Attachments | OT STRATEGY x DUPLICATION x USA | FDA UDI | Class I | Active |
| Sphero Flex | S/FLEX PRIMA CONNEX ø 4,1 h.5 TiN | FDA UDI | Class II | Active |
| Sphero Flex | SET S.FLEX CALC INT-OMN ø3.25 h6 | FDA UDI | Class II | Active |
| Sphero Block Micro | S/BLOCK MICRO CERTAIN 3I ø 3,25 h.4 TiN | FDA UDI | Class II | Active |
| Sphero Block Micro | SPHERO BLOCK Micro CORE VENT h.3 RIV.TiN | FDA UDI | Class II | Active |
| Ot Equator Titanium Abutment | OT EQUATOR BRANEMARK NP H 4 | FDA UDI | Class II | Unknown |
| Sphero Block Micro | S/BLOCK MICRO ReplaceSelect ø4.3 h.1 TiN | FDA UDI | Class II | Unknown |
| Endodontic Posts | INTRODUCTORY SET | FDA UDI | Class I | Active |
| OT Equator | Set OT Equator EZTETIC ø 3,1 h.1 | FDA UDI | Class II | Active |
| Ot Equator Titanium Abutment | ASTRA TECH LILAC H 3 | FDA UDI | Class II | Active |
| Ot Equator - Ot Bridge | OT EQUATOR N BONE LEVEL SC ø 2,9 h.3 | FDA UDI | 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