Data / Medical devices / United States / Pipeline Medical Products, LLC
Pipeline Medical Products, LLC: FDA-registered device maker in Weymouth, MA, United States, 1 510(k) clearance
Pipeline Medical Products, LLC is registered with the FDA (registration 3041679947) in Weymouth, MA, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated August 13, 2025. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 3041679947
- Address
- 122 Park Ave, Weymouth, MA, United States, 02190
- Owner or operator
- Pipeline Medical Products, LLC (10094095)
- Roles
- Specification developer
- First device listed
- November 14, 2025
- Registered through
- 2026
- Brand names listed
- Aero Jet Ventilation Catheter
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Tube, Tracheal (W/Wo Connector) | BTR | 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 |
|---|---|---|---|---|---|---|
| August 13, 2025 | K243579 | AeroJet Ventilation Catheter | BTR | Substantially Equivalent | Pipeline Medical Products, LLC | accessdata.fda.gov |
Compare with other makers
Updated August 13, 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.