# Moss Tubes, Inc.

- Location (FDA's records): Elizabeth, NJ
- FDA decisions: 5 (1999–2019): 5 510(k) clearances
- Product codes: KNT (3), BSS (1), PIF (1)
- Predicates its devices cite: 2 (2 its own); citations of its devices by later devices: 3 (2 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Turboseal, L.P.: 1 (https://510kreport.com/company/turboseal)

## Its most-cited devices
- K984629: Moss Tubes, Inc. Nasal Tube - Mark IV (1999), cited by 2
- K990389: Moss Gastrostomy Tube (1999), cited by 1

## Recent decisions
- K190414: Moss Gastrostomy Tube, Moss Nasal Tube – Mark IV (Jun 14, 2019)
- K990389: Moss Gastrostomy Tube (Mar 22, 1999)
- K984628: Modification of Moss P.E.G. Tray (Mar 17, 1999)
- K984629: Moss Tubes, Inc. Nasal Tube - Mark IV (Mar 2, 1999)
- K984310: Moss Tubes, Inc, All Silicone Gastrostomy Tube (Feb 24, 1999)

Source page: https://510kreport.com/company/moss-tubes