Data / Medical devices / Italy / World Work SRL
World Work SRL: FDA-registered device maker in MONTEBELLO VICENTINO Vicenza, Italy, 1 510(k) clearance
World Work SRL is registered with the FDA (registration 3006153346) in MONTEBELLO VICENTINO Vicenza, Italy. It lists 4 device types. The FDA files 1 510(k) clearance under its listings, the newest dated May 1, 2023. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3006153346
- Address
- Via Del Progresso, 47, MONTEBELLO VICENTINO Vicenza, Italy, 36054
- Owner or operator
- WORLD WORK SRL (9090471)
- Roles
- Manufacturer
- First device listed
- August 1, 2006
- Registered through
- 2026
- Brand names listed
- ALLOY, AMALGAM DENTAL AMALGAM, CAPSULES, DENTAL AMALGAM, Mouthpiece, saliva ejector
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Alloy, Amalgam | EJJ | 2 | Manufacturer | accessdata.fda.gov |
| Capsule, Dental, Amalgam | DZS | 1 | Manufacturer | accessdata.fda.gov |
| Dental Amalgam | OIV | 2 | Manufacturer | accessdata.fda.gov |
| Mouthpiece, Saliva Ejector | DYN | 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 |
|---|---|---|---|---|---|---|
| May 1, 2023 | K223182 | Arial Dental, Mistral Dental Amalgam, World Work Dental Amalgam, BMS Non Gamma 2 Alloy, Flexi Alloy, Hi-S Alloy, WW Dental Amalgam, Hi - Mix, Non Gamma 2 Alloy | OIV | Substantially Equivalent | Worldwork S.R.L | accessdata.fda.gov |
Compare with other makers
- All makers of Alloy, Amalgam
- All makers of Dental Amalgam
- All makers of Mouthpiece, Saliva Ejector
- All makers of Capsule, Dental, Amalgam
Updated May 1, 2023. 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.