# L&Z Us, Inc.

- Location (FDA's records): Norwood, NJ
- FDA decisions: 6 (2016–2023): 6 510(k) clearances
- Product codes: LJS (6)
- 510(k) review time since 2016: median 47 days, against 74 for FDA's reviews in the same codes and years (3 of 6 faster)
- Predicates its devices cite: 1 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Navilyst Medical, Inc.: 1 (https://510kreport.com/company/navilyst-medical)

## Recent decisions
- K233149: CATHTONG III Tapered PICC Catheter (Dec 1, 2023)
- K232571: CATHTONG™ II PICC Catheter (Sep 22, 2023)
- K232594: CATHTONG™ II PICC Catheter (Sep 22, 2023)
- K172039: CATHTONG II PICC Catheter (Aug 3, 2017)
- K170486: CATHTONG II PICC Catheter (May 25, 2017)
- K153469: Cathtong I PICC Catheter (Sep 1, 2016)

Source page: https://510kreport.com/company/l-z-us