Data / Medical devices / Pneumoperitoneum Needle / United States
FDA-registered makers of Pneumoperitoneum Needle in the United States: 9 establishments
9 establishments in the United States are registered with the FDA to make Pneumoperitoneum Needle (product code FHO). 7 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
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- Device
- Pneumoperitoneum Needle
- Product code
- FHO
- Country
- United States
Makers of Pneumoperitoneum Needle in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Conmed Corporation | Utica, NY, United States | Complaint file establishment, Manufacturer | 1 | November 27, 1991 | 0 | 0 | 0 | api.fda.gov |
| Coopersurgical, Inc. | Trumbull, CT, United States | Manufacturer | 1 | March 27, 1997 | 0 | 0 | 0 | api.fda.gov |
| ConMed Corporation | Greenwood Village, CO, United States | Specification developer | 1 | November 27, 1991 | 0 | 0 | 0 | api.fda.gov |
| Covidien | North Haven, CT, United States | Contract manufacturer, Manufacturer, Specification developer | 1 | October 2, 1986 | 0 | 0 | 0 | api.fda.gov |
| Covidien | Ponce, PR, United States | Contract manufacturer, Manufacturer | 1 | October 2, 1986 | 0 | 0 | 0 | api.fda.gov |
| Medtronic Distribution Center | Memphis, TN, United States | Manufacturer | 1 | October 2, 1986 | 0 | 0 | 0 | api.fda.gov |
| Ranfac Corp. | Avon, MA, United States | Contract manufacturer, Manufacturer | 1 | July 23, 1993 | 0 | 0 | 0 | api.fda.gov |
| Geotec, Inc. | Warwick, RI, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| MEDLINE INDUSTRIES, LP - Northfield | Northfield, IL, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 2, 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.