# Glw, Inc.

- Location (FDA's records): Englewood Cliff, NJ
- FDA decisions: 3 (2021–2023): 3 510(k) clearances
- Product codes: HSB (2), HWC (1)
- 510(k) review time since 2016: median 157 days, against 104 for FDA's reviews in the same codes and years (2 of 3 faster)
- Predicates its devices cite: 7 (1 its own); citations of its devices by later devices: 1 (1 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
- Glw Medical, Inc.: 3 (https://510kreport.com/company/glw-medical)
- Howmedica Osteonics Corp.: 2 (https://510kreport.com/company/howmedica-osteonics)
- Biomet, Inc.: 1 (https://510kreport.com/company/biomet)

## Its most-cited devices
- K201379: Artemis Proximal Femoral Nail System (2021), cited by 1

## Recent decisions
- K223847: CREED™ Cannulated Screws (Jan 25, 2023)
- K221489: Artemis Proximal Femoral Nail System (Oct 27, 2022)
- K201379: Artemis Proximal Femoral Nail System (Feb 19, 2021)

Source page: https://510kreport.com/company/glw