Data / Medical devices / United States / Moss Tubes, Inc.
Moss Tubes, Inc.: FDA-registered device maker in Castleton on Hudson, NY, United States, 5 510(k) clearances
Moss Tubes, Inc. is registered with the FDA (registration 1320599) in Castleton on Hudson, NY, United States. It lists 2 device types. The FDA files 5 510(k) clearances under its listings, the newest dated March 22, 1999. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 1320599
- FEI number
- 3000717944
- Address
- 1929 Route 9, Castleton on Hudson, NY, United States, 12033
- Owner or operator
- MOSS TUBES, INC. (9029281)
- Roles
- Manufacturer, Specification developer
- First device listed
- November 29, 2007
- Registered through
- 2026
- Brand names listed
- All Silicone Gastrostomy Tube, Moss Anchor Set, Moss Gastrostomy Tube, Moss Nasal Tube Mark IV, Moss PEG Kit, Moss Simplified PEG Kit
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Tube, Nasogastric | BSS | 2 | Manufacturer | accessdata.fda.gov |
| Tubes, Gastrointestinal (And Accessories) | KNT | 2 | Manufacturer, 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 |
|---|---|---|---|---|---|---|
| March 22, 1999 | K990389 | MOSS GASTROSTOMY TUBE | KNT | Substantially Equivalent | Moss Tubes, Inc. | accessdata.fda.gov |
| March 17, 1999 | K984628 | MODIFICATION OF MOSS P.E.G. TRAY | KNT | Substantially Equivalent | Moss Tubes, Inc. | accessdata.fda.gov |
| March 2, 1999 | K984629 | MOSS TUBES, INC. NASAL TUBE - MARK IV | BSS | Substantially Equivalent | Moss Tubes, Inc. | accessdata.fda.gov |
| February 24, 1999 | K984310 | MOSS TUBES, INC, ALL SILICONE GASTROSTOMY TUBE | KNT | Substantially Equivalent | Moss Tubes, Inc. | accessdata.fda.gov |
| June 24, 1991 | K910910 | MOSS- ANCHOR SET | KNT | Substantially Equivalent | Moss Medical Products | accessdata.fda.gov |
Compare with other makers
Updated March 22, 1999. 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.