Data / Medical devices / United States / Bonago Medical Solutions LLC Dba Renovatio
Bonago Medical Solutions LLC Dba Renovatio: FDA-registered device maker in Miami, FL, United States, 2 510(k) clearances
Bonago Medical Solutions LLC Dba Renovatio is registered with the FDA (registration 3023274465) in Miami, FL, United States. It lists 3 device types. The FDA files 2 510(k) clearances under its listings, the newest dated January 8, 2025. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 3023274465
- Address
- 7448 Sw 48th St, Miami, FL, United States, 33155
- Owner or operator
- Bonago Medical Solutions LLC dba Renovatio (10085632)
- Roles
- Repackager or relabeler
- First device listed
- April 17, 2026
- Registered through
- 2026
- Brand names listed
- CANNULALL, Cannulall, Renovatio, Renovatio PDO
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Needle, Aspiration And Injection, Disposable | GAA | 1 | Repackager or relabeler | accessdata.fda.gov |
| Needle, Hypodermic, Single Lumen | FMI | 2 | Repackager or relabeler | accessdata.fda.gov |
| Suture, Surgical, Absorbable, Polydioxanone | NEW | 2 | Repackager or relabeler | 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 8, 2025 | K242741 | ACE Cannula | FMI | Substantially Equivalent | Ace Medical Industry Co., Ltd. | accessdata.fda.gov |
| November 22, 2016 | K160761 | DW-1C | NEW | Substantially Equivalent | Dongwon Medical Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Needle, Hypodermic, Single Lumen
- All makers of Needle, Aspiration And Injection, Disposable
- All makers of Suture, Surgical, Absorbable, Polydioxanone
Updated January 8, 2025. 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.