Data / Medical devices / United States / Seaside Marine International Drug Co., Inc.
Seaside Marine International Drug Co., Inc.: FDA-registered device maker in San Pedro, CA, United States, 2 510(k) clearances
Seaside Marine International Drug Co., Inc. is registered with the FDA (registration 3011767915) in San Pedro, CA, United States. It lists 4 device types. The FDA files 2 510(k) clearances under its listings, the newest dated February 11, 2011. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 3011767915
- Address
- 599 W 7TH ST, San Pedro, CA, United States, 90731
- Owner or operator
- Seaside Marine International Drug Co., Inc. (10049653)
- Roles
- Repackager or relabeler
- First device listed
- January 5, 2026
- Registered through
- 2026
- Brand names listed
- FAK360
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Generator, Oxygen, Portable | CAW | 2 | Repackager or relabeler | accessdata.fda.gov |
| Kit, First Aid, Talking | OVR | 1 | Repackager or relabeler | accessdata.fda.gov |
| Splint, Extremity, Non-Inflatable, External, Non-Sterile | NOC | 1 | Repackager or relabeler | accessdata.fda.gov |
| Valve, Non-Rebreathing | CBP | 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 |
|---|---|---|---|---|---|---|
| February 11, 2011 | K102750 | O2-IN-A-BOX, O2-IN-A-BOX | CAW | Substantially Equivalent | Geto2, Inc. | accessdata.fda.gov |
| April 8, 1997 | K963755 | SPIRACLE TECHNOLOGY - MODEL 302 OX INHALATOR | CBP | Substantially Equivalent | Spiracle Technology | accessdata.fda.gov |
Compare with other makers
- All makers of Generator, Oxygen, Portable
- All makers of Valve, Non-Rebreathing
- All makers of Splint, Extremity, Non-Inflatable, External, Non-Sterile
- All makers of Kit, First Aid, Talking
Updated February 11, 2011. 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.