Data / Medical devices / United States / Sutura Medical Technologies LLC
Sutura Medical Technologies LLC: FDA-registered device maker in Miami, FL, United States, 1 510(k) clearance
Sutura Medical Technologies LLC is registered with the FDA (registration 3030141376) in Miami, FL, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated June 12, 2026. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3030141376
- Address
- 2121 Sw 3rd Ave Ste 500, Miami, FL, United States, 33129
- Owner or operator
- Sutura Medical Technologies LLC (10096134)
- Roles
- Specification developer
- First device listed
- July 6, 2026
- Registered through
- 2026
- Brand names listed
- Sutura PDO Suture
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Suture, Surgical, Absorbable, Polydioxanone | NEW | 2 | Specification developer | 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 |
|---|---|---|---|---|---|---|
| June 12, 2026 | K252171 | Barbed PDO Suture | NEW | Substantially Equivalent | Sutura Medical Technology, Inc. | accessdata.fda.gov |
Compare with other makers
Updated June 12, 2026. 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.