Data / Medical devices / Italy / Orthodontic Manufacturer Sia SRL
Orthodontic Manufacturer Sia SRL: FDA-registered device maker in ROCCA D EVANDRO Caserta, Italy, 1 510(k) clearance
Orthodontic Manufacturer Sia SRL is registered with the FDA (registration 9710113) in ROCCA D EVANDRO Caserta, Italy. It lists 15 device types. The FDA files 1 510(k) clearance under its listings, the newest dated July 10, 1996. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 9710113
- FEI number
- 3003348399
- Address
- Zona Industriale Via Vandra, ROCCA D EVANDRO Caserta, Italy, 81040
- Owner or operator
- ORTHODONTIC MANUFACTURER SIA SRL (9080887)
- Roles
- Manufacturer
- First device listed
- March 19, 2001
- Registered through
- 2026
- Brand names listed
- ACTIVA, BT2 - BITURBO, CRIMPABLE STOP, D-bar, FACEBOW, HEXAGON, I-ARCH, INTERPROXIMAL INCREMENTAL GAUGE and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Band, Elastic, Orthodontic | ECI | 1 | Manufacturer | accessdata.fda.gov |
| Band, Material, Orthodontic | DYO | 1 | Manufacturer | accessdata.fda.gov |
| Band, Preformed, Orthodontic | ECM | 1 | Manufacturer | accessdata.fda.gov |
| Bracket, Metal, Orthodontic | EJF | 1 | Manufacturer | accessdata.fda.gov |
| Clamp, Wire, Orthodontic | ECN | 1 | Manufacturer | accessdata.fda.gov |
| Facebow | KCR | 1 | Manufacturer | accessdata.fda.gov |
| Gauge, Depth, Instrument, Dental | EIL | 1 | Manufacturer | accessdata.fda.gov |
| Headgear, Extraoral, Orthodontic | DZB | 2 | Manufacturer | accessdata.fda.gov |
| Maintainer, Space Preformed, Orthodontic | DYT | 1 | Manufacturer | accessdata.fda.gov |
| Plier, Orthodontic | JEX | 1 | Manufacturer | accessdata.fda.gov |
| Pusher, Band, Orthodontic | ECS | 1 | Manufacturer | accessdata.fda.gov |
| Retainer, Screw Expansion, Orthodontic | DYJ | 1 | Manufacturer | accessdata.fda.gov |
| Spring, Orthodontic | ECO | 1 | Manufacturer | accessdata.fda.gov |
| Tube, Orthodontic | DZD | 1 | Manufacturer | accessdata.fda.gov |
| Wire, Orthodontic | DZC | 1 | 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 |
|---|---|---|---|---|---|---|
| July 10, 1996 | K961754 | SAFETY RELEASE MODULE | DZB | Substantially Equivalent | G & H Wire Co. | accessdata.fda.gov |
Compare with other makers
- All makers of Clamp, Wire, Orthodontic
- All makers of Spring, Orthodontic
- All makers of Band, Preformed, Orthodontic
- All makers of Gauge, Depth, Instrument, Dental
- All makers of Facebow
- All makers of Retainer, Screw Expansion, Orthodontic
Updated July 10, 1996. 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.