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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 74 of 89| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Ot Equator - Ot Bridge | OT EQUATOR ASTRA LILLA ø 4,5-5-5S h.5 | FDA UDI | Class II | Active |
| Sphero Flex | S/FLEX AB Int/Hex Narrow h.2 TiN | FDA UDI | Class II | Unknown |
| Ot Equator Titanium Abutment | BONE LEVEL NC H 6 | FDA UDI | Class II | Unknown |
| Ot Equator - Ot Bridge | PINK CAP MICRO #100 | FDA UDI | Class I | Active |
| Ot Equator - Ot Bridge | OT EQUATOR MINI MN ø 3 h.4 c/SmartBox | FDA UDI | Class II | Active |
| Sphero Block Normo | SPHERO BLOCK NORMO EZTETIC ø 3,1 h.1 | FDA UDI | Class II | Active |
| Ot Equator Titanium Abutment | OT EQUATOR PREMIUM KHONO ø 3,8 h.1 | FDA UDI | Class II | Active |
| Sphero Block Normo | S/BLOCK N ASTRA ST ø 4 h.3 TiN | FDA UDI | Class II | Unknown |
| Ot Equator Titanium Abutment | ANKYLOS CX H 7 | FDA UDI | Class II | Active |
| Sphero Block Normo | S/BLOCK N BIO HORIZONS ø 3 h.7 TiN | FDA UDI | Class II | Active |
| Dental Equipments | S/STEEL HOUSING STANDARD size 100 u. | FDA UDI | Class I | Unknown |
| Endodontic Posts | PIVOT tit. EQUATOR mm.9 set | FDA UDI | Class I | Active |
| Ot Equator-Ot Bridge | MINI EXTRAGR. Ø3,5 TIT. AB. W/SCREW & SEEG. | FDA UDI | Class I | Active |
| Ot Equator Titanium Abutment | REPLACE SELECT NP H 2 | FDA UDI | Class II | Unknown |
| Ot Equator-Ot Bridge | ODSecure Analog 500 u. | FDA UDI | Class I | Unknown |
| Sphero Block Micro | SPHERO BLOCK MICRO STRAUMANN ITI h.2 TiN | FDA UDI | Class II | Unknown |
| Ot Equator Titanium Abutment | OT EQUATOR ASTRA EV ø 4,8 h.5 c/SB | FDA UDI | Class II | Active |
| Ot Equator Titanium Abutment | OT EQUATOR N BONE LEVEL SC ø 2,9 h.4 | FDA UDI | Class II | Active |
| Ot Equator-Ot Bridge | OT EQUATOR STERI OSS E/E ø 3,25 h.3 c/SB | FDA UDI | Class I | Unknown |
| Sphero Block Normo | S.BLOCK N. SCREW VENT ø 5,7 h.2 TiN | FDA UDI | Class II | Active |
| OT Equator | Set OT EQUATOR INDEX Std e Wide +Smartbox h.0,5 | FDA UDI | Class II | Active |
| Ot Equator Titanium Abutment | OT EQUATOR REPLACE SELECT NP H 7 | FDA UDI | Class II | Active |
| Ot Equator Titanium Abutment | FRIALIT XIVE DIAMETER 4,5 H 4 | FDA UDI | Class II | Unknown |
| Ot Equator Titanium Abutment | FRIALIT XIVE DIAMETER 3,8 H 1 | FDA UDI | Class II | Unknown |
| Sphero Block Normo | S/B/NORMO BONE LEVEL NC ø 3,3 h.5 TiN | FDA UDI | Class II | Unknown |
| Ot Equator-Ot Bridge | OT EQUATOR ASTRA EV ø 4,8 h.5 | FDA UDI | Class I | Unknown |
| Ot Equator-Ot Bridge | OT EQUATOR h.0,5 (as yr.sample) | FDA UDI | Class I | Unknown |
| Sphero Block Normo | S/ BLOCK N MINI MN ø 3-3,25 h.4 TiN | FDA UDI | Class II | Unknown |
| Ot Equator Titanium Abutment | BRANEMARK WP DIAMETER 5 H 4 | FDA UDI | Class II | Unknown |
| OT Equator | Set OT Equator S.P.I ø 5 + Smartbox h.3 | FDA UDI | Class II | Active |
| OT Equator | Set OT Equator TiRADIX ø 3.75-4-4.5 h.1 | FDA UDI | Class II | Active |
| OT Equator | Set OT Equator S.P.I ø 5 h.3 | FDA UDI | Class II | Active |
| Sphero Block Micro | S/BLOCK MICRO CERTAIN 3I ø4,1 h.4TiN | FDA UDI | Class II | Unknown |
| Sphero Flex | SPHERO FLEX BRANEMARK ø 3,3 h.1,1 TiN | FDA UDI | Class II | Unknown |
| Sphero Block Normo | S/B/NORMO BONE LEVEL NC ø 3,3 h.4 TiN | FDA UDI | Class II | Unknown |
| Sphero Block Normo | S/ B/NORMO ENDURE Imtec ø 3,5-4,3 h.3TiN | FDA UDI | Class II | Unknown |
| OT Equator | OT EQUATOR CoAxis H/E ø 5 h.2 | FDA UDI | Class II | Active |
| Ot Equator Titanium Abutment | SCREW VENT DIAMETER 3,5 H 0,5 | FDA UDI | Class II | Unknown |
| Sphero Block Micro | S/BLOCK MICRO CERTAIN 3I ø 3,25 h.5 TiN | FDA UDI | Class II | Unknown |
| OT Equator | Set OT Equator PREMIUM KHONO ø 5 + Smartbox h.5 | FDA UDI | Class II | Active |
| OT Equator | OT EQUATOR CoAxis H/E ø 3,25 +Smartbox h.7 | FDA UDI | Class II | Active |
| OT Equator | OT EQUATOR PREMIUM KHONO ø 3,8 h.5 | FDA UDI | Class II | Active |
| OT Equator | Set OT Equator GL Impl/System C-TECH h.3 | FDA UDI | Class II | Active |
| OT Equator | OT EQUATOR ASTRA EV ø 3,6 h.5 | FDA UDI | Class II | Active |
| OT Equator | Set OT Equator KONTACT ø 3 h.1,2 | FDA UDI | Class II | Active |
| Ot Equator Titanium Abutment | NOBEL ACTIVE RP H 6 | FDA UDI | Class II | Active |
| OT Equator | OT Equator SW MORSE h.3 | FDA UDI | Class II | Active |
| Ot Equator Titanium Abutment | REACTIVE-REPLUS DIAMETER 5 H 4 | FDA UDI | Class II | Active |
| Sphero Block Normo | SPHERO BLOCK ASTRA EV ø 5,4 h.1 TIN | FDA UDI | Class II | Active |
| OT Equator | Set OT Equator IMTEC ENDURE ø 3,5-4,3 h.2 | 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