Is this your brand? Sign in to claim ownership.
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
- —
- Website
- —
- —
- —
- —
- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 439240722
Catalogue (4428)
Page 14 of 89| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Ot Equator - Ot Bridge | EQUATOR TITANIUM HOUSINGS 2 units | FDA UDI | Class I | Active |
| OT Equator | OT EQUATOR IMTEC ENDURE ø 3,5-4,3 h.1 | FDA UDI | Class II | Active |
| OT Equator | Set OT Equator CoAxis H/E ø 4 h.2 | FDA UDI | Class II | Active |
| Sphero Block Micro | S/BLOCK MICRO ReplaceSelect ø4.3 h.2 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 | Active |
| Ot Equator-Ot Bridge | OT EQUATOR STRAUMANN h.2 c/Smart Box | FDA UDI | Class I | Unknown |
| Ot Equator Titanium Abutment | REPLACE SELECT NP H 7 | FDA UDI | Class II | Active |
| Sphero Block Micro | S/BLOCK MICRO ReplaceSelect ø4.3 h.1 TiN | FDA UDI | Class II | Active |
| Sphero Block Micro | SPHERO B/M ReplaceSelect ø4.3 h0,5 TIN | FDA UDI | Class II | Active |
| Ot Equator Titanium Abutment | OT EQUATOR ASTRA EV ø 3,6 h.2 | FDA UDI | Class II | Active |
| Ot Equator-Ot Bridge | OT EQUATOR CERTAIN ø 5 h.4 | FDA UDI | Class I | Unknown |
| Ot Equator-Ot Bridge | OT EQUATOR BRANEMARK h.4 | FDA UDI | Class I | Unknown |
| Ot Equator Titanium Abutment | OT EQUATOR REPLACE SELECT WP H 0,5 | FDA UDI | Class II | Active |
| Sphero Block Normo | S/BLOCK NORMO INTEG/OMNIL. ø 3,25 h.4TiN | FDA UDI | Class II | Unknown |
| OT Equator | OT EQUATOR LUNA RP h.5 | FDA UDI | Class II | Active |
| Ot Equator Titanium Abutment | BRANEMARK NP H 5 | FDA UDI | Class II | Unknown |
| Ot Equator-Ot Bridge | OT EQUATOR SCAN ABUTMENT W/SCREW | EUDAMEDFDA UDI | Class I | Active |
| Ot Equator - Ot Bridge | Set OT EQUATOR ReplaceSelect ø 4,3 +Smartbox h.4 | FDA UDI | Class II | Active |
| Dental Attachments | POSITIONING PIVOTS PLAS/MODEL MICRO x2 | FDA UDI | Class I | Unknown |
| Ot Equator Titanium Abutment | OT Equator GH 4.5 | FDA UDI | Class II | Active |
| Sphero Block Micro | S/B/MICRO BONE LEVEL NC ø 3,3 h.5 TiN | FDA UDI | Class II | Unknown |
| OT Equator | Set OT Equator PREMIUM ø 3,3 + Smartbox h.2 | FDA UDI | Class II | Active |
| Ot Equator-Ot Bridge | ODSECURE TITANIUM COPING, NARROW | FDA UDI | Class I | Active |
| OT Equator | Set OT Equator OSSEOLINK ø 3,5-4-5 h.2 | FDA UDI | Class II | Active |
| Ot Equator Titanium Abutment | BONE LEVEL NC H 2 | FDA UDI | Class II | Unknown |
| Sphero Block Normo | SPHERO BLOCK N SCREW VENT h.1 TiN | FDA UDI | Class II | Active |
| Ot Equator Titanium Abutment | OT EQUATOR BRANEMARK RP H 2 | FDA UDI | Class II | Unknown |
| Ot Equator Titanium Abutment | OT EQUATOR BONE LEVEL RC H 2 | FDA UDI | Class II | Unknown |
| Ot Equator-Ot Bridge | OT EQUATOR BRK/Restore WP ø 5 h.2 | FDA UDI | Class I | Unknown |
| Dental Equipments | S/STEEL HOUSING STD. size 50 u. | FDA UDI | Class I | Active |
| Ot Equator Titanium Abutment | CERTAIN 3i DIAMETER 3,25 H 3 | FDA UDI | Class II | Active |
| Ot Equator-Ot Bridge | OT EQUATOR LITTLE IMPLANT ø 3,5 h.4 | FDA UDI | Class I | Unknown |
| Sphero Block Micro | S/BLOCK Micro STERI OSS ø 3,25 h.2 TiN | FDA UDI | Class II | Unknown |
| OT Equator | Set OT Equator KONTACT ø 3 h.6 | FDA UDI | Class II | Active |
| Ot Equator Titanium Abutment | ASTRA TECH AQUA H 0 | FDA UDI | Class II | Unknown |
| Ot Equator - Ot Bridge | OT EQUATOR BIO HORIZONS ø 4 h.2 | FDA UDI | Class II | Active |
| Ot Equator-Ot Bridge | OT EQUATOR BONE LEVEL RC ø 4,1-4,8 h.7 | FDA UDI | Class I | Unknown |
| Sphero Block Micro | S/BLOCK MICRO SCREW VENT ø 5,7 h.7 TiN | FDA UDI | Class II | Active |
| Ot Equator Titanium Abutment | NOBEL ACTIVE NP H 5 | FDA UDI | Class II | Unknown |
| Ot Equator-Ot Bridge | OT EQUATOR ASTRA ST ø 4 h.1 | FDA UDI | Class I | Unknown |
| Invasive Accessories And Instruments | ESTRATTORE IMP. CERTAIN 3i ø 3,25 | FDA UDI | Class I | Active |
| Sphero Flex | SPHERO FLEX CORE VENT h.2 RIV.TiN | FDA UDI | Class II | Active |
| Ot Equator-Ot Bridge | OT EQUATOR Frialit 2 ø 3 h.1 | FDA UDI | Class I | Unknown |
| Ot Equator-Ot Bridge | OT EQUATOR ReplaceSelect ø 3,5 h.0,5 | FDA UDI | Class I | Unknown |
| Sphero Block Normo | S/ BLOCK NORMO REPL/SELECT ø 3,5 h.4 TiN | FDA UDI | Class II | Active |
| dental attachments | TITAN CAP MICRO size pz.2 | FDA UDI | Class I | Active |
| Ot Equator Titanium Abutment | OT EQUATOR ASTRA EV ø 3,6 h.7 | FDA UDI | Class II | Active |
| Ot Equator-Ot Bridge | OT EQUATOR SMART BOX 1 unit | FDA UDI | Class I | Unknown |
| Ot Equator Titanium Abutment | OT EQUATOR BRANEMARK WP DIAMETER 6 H 2 | FDA UDI | Class II | Active |
| Ot Equator Titanium Abutment | BRANEMARK WP DIAMETER 6 H 7 | FDA UDI | Class II | Unknown |
Related Companies
Authorised Representatives
No authorised representatives on record.
Importers
Not available yet.
Notified Bodies
Not available yet.
Authorities
Not available yet.
FDA Establishments (1)
Establishments registered with the FDA under this company group, matched by name.
- Rhein 83 Srl BOLOGNA Emilia-Romagna · IT FEI 3002807996