Data / Medical devices / Brazil / Alliage S/A Industrias Medico Odontologica
Alliage S/A Industrias Medico Odontologica: FDA-registered device maker in Ribeirao Preto Sao Paulo, Brazil, 8 510(k) clearances
Alliage S/A Industrias Medico Odontologica is registered with the FDA (registration 3002819275) in Ribeirao Preto Sao Paulo, Brazil. It lists 10 device types. The FDA files 8 510(k) clearances under its listings, the newest dated January 3, 2024. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 3002819275
- Address
- Rodovia Abrao Assed Km 53+450 metros Recreio Anhanguera, Ribeirao Preto Sao Paulo, Brazil, 14097-500
- Owner or operator
- Alliage S/A Industrias Medico Odontologica (10024158)
- Roles
- Manufacturer
- First device listed
- October 30, 2008
- Registered through
- 2026
- Brand names listed
- 1335 Chair Mounted Light, 1340MD Ceilng Mounted Light, 1340MD Chair Mounted Light, 1340MD Wall Mounted Light, 1402 2 HP All-in-one Delivery Unit, 1402 2 HP Delivery Unit, 1403 2HP Dual Mount Unit, 1407 3 HP Delivery Unit and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Chair, Dental, With Operative Unit | KLC | 1 | Manufacturer | accessdata.fda.gov |
| Chair, Examination And Treatment | FRK | 1 | Manufacturer | accessdata.fda.gov |
| Intraoral Camera | QJK | 2 | Manufacturer | accessdata.fda.gov |
| Light, Operating, Dental | EAZ | 1 | Manufacturer | accessdata.fda.gov |
| Solid State X-Ray Imager (Flat Panel/Digital Imager) | MQB | 2 | Manufacturer | accessdata.fda.gov |
| System, X-Ray, Extraoral Source, Digital | MUH | 2 | Manufacturer | accessdata.fda.gov |
| Unit, Operative Dental | EIA | 1 | Manufacturer | accessdata.fda.gov |
| Unit, Syringe, Air And/Or Water | ECB | 1 | Manufacturer | accessdata.fda.gov |
| Unit, X-Ray, Extraoral With Timer | EHD | 2 | Manufacturer | accessdata.fda.gov |
| X-Ray, Tomography, Computed, Dental | OAS | 2 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| January 3, 2024 | K233395 | Portable Dental X-Ray (AXR60 S); Portable Dental X-Ray (AXR65 S) | EHD | Substantially Equivalent | Alliage S/A Industrias Médico Odontológica | accessdata.fda.gov |
| April 11, 2023 | K230732 | Eagle S/Saevo Slim/D700 Slim | MUH | Substantially Equivalent | Alliage S/A Industrias Medica Odontológico. | accessdata.fda.gov |
| April 7, 2023 | K223816 | Dental CT Scanner AXR | OAS | Substantially Equivalent | Alliage S/A Industrias Medico Odontológica | accessdata.fda.gov |
| August 10, 2021 | K210820 | EAGLE EDGE AXR90 and AXR120 | OAS | Substantially Equivalent | Alliage S/A Industrias Medico Odontológica | accessdata.fda.gov |
| January 22, 1997 | K964619 | DELIVERY SYSTEM(SDS 1400 XL)/DELIVERY SYSTEM CUSPIDOR(SDS1450,SDS1650 XL) | EIA | Substantially Equivalent | Sds Dental, Inc. | accessdata.fda.gov |
| October 1, 1986 | K863021 | CM-II, CM-I WATER UNIT | EIA | Substantially Equivalent | Sds Dental, Inc. | accessdata.fda.gov |
| October 1, 1986 | K863016 | DENTATUS L SET | KLC | Substantially Equivalent | Sds Dental, Inc. | accessdata.fda.gov |
| September 29, 1986 | K863019 | F-11 REFLECTOR / F-II STANDARD REFLECTOR | EAZ | Substantially Equivalent | Sds Dental, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Unit, Operative Dental
- All makers of Chair, Dental, With Operative Unit
- All makers of Intraoral Camera
- All makers of Light, Operating, Dental
- All makers of Chair, Examination And Treatment
- All makers of X-Ray, Tomography, Computed, Dental
Updated January 3, 2024. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.