Data / Medical devices / United States / Poseidon Medical Inc.
Poseidon Medical Inc.: FDA-registered device maker in Pembroke Pines, FL, United States, 1 PMA approval
Poseidon Medical Inc. is registered with the FDA (registration 3016248656) in Pembroke Pines, FL, United States. It lists 1 device type. The FDA files 1 PMA approval under its listings, the newest dated February 21, 2017. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 3016248656
- Address
- 1125 NW 132nd Avenue, Pembroke Pines, FL, United States, 33028
- Owner or operator
- Poseidon Medical Inc. (10062215)
- Roles
- Specification developer
- First device listed
- December 30, 2019
- Registered through
- 2026
- Brand names listed
- Tryton Side Branch Stent
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Stent, Coronary | MAF | 3 | Specification developer | accessdata.fda.gov |
PMA approvals
Premarket approvals this establishment lists, with the supplements the FDA has decided since.
| Approved | PMA number | Device | Product code | Supplements | Latest decision | Source |
|---|---|---|---|---|---|---|
| February 21, 2017 | P150039 | TRYTON SIDE BRANCH STENT | MAF | 5 | October 4, 2020 | accessdata.fda.gov |
Compare with other makers
Updated October 4, 2020. 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.