# Relign Corporation

- Location (FDA's records): Campbell, CA
- FDA decisions: 2 (2017–2023): 2 510(k) clearances
- Product codes: GEI (2)
- Predicates its devices cite: 3 (1 its own); citations of its devices by later devices: 3 (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
- Stryker Endoscopy: 2 (https://510kreport.com/company/stryker-endoscopy)

## Firms that cite its devices most
- Relign Corporation, Subsidiary of Zimmer Biomet: 2 (https://510kreport.com/company/relign-subsidiary-of-zimmer-biomet)

## Its most-cited devices
- K162770: Relign System (2017), cited by 2
- K233493: Tricera Arthroscopic System; Tricera Controller (R-10001); Tricera Shaver Handpiece (R-10023); Veriflow (R-10003); Exoflow (R-10017); 3-in-1 Shaver 4.2mm (R-10008); 3-in-1 Shaver 5.0mm (R-10014); Dynablator (R-10005); Standard Burr (R-10021); Standard Shaver 3.4mm (R-10012); Curved Standard Shaver 3.4mm (R-10024) (2023), cited by 1

## Recent decisions
- K233493: Tricera Arthroscopic System; Tricera Controller (R-10001); Tricera Shaver Handpiece (R-10023); Veriflow (R-10003); Exoflow (R-10017); 3-in-1 Shaver 4.2mm (R-10008); 3-in-1 Shaver 5.0mm (R-10014); Dynablator (R-10005); Standard Burr (R-10021); Standard Shaver 3.4mm (R-10012); Curved Standard Shaver 3.4mm (R-10024) (Nov 28, 2023)
- K162770: Relign System (Jan 4, 2017)

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