# Relign Corporation, Subsidiary of Zimmer Biomet

- Location (FDA's records): Campbell, CA
- FDA decisions: 1 (2024–2024): 1 510(k) clearance
- Product codes: GEI (1)
- Predicates its devices cite: 2 (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
- Relign Corporation: 2 (https://510kreport.com/company/relign)

## Recent decisions
- K241008: Tricera Arthroscopic System; Tricera Controller (R-10001); Tricera Handpiece, Autoclavable  (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 5.0mm (R-10021); Standard Shaver 3.4mm (R-10012); Curved Standard Shaver 3.4mm (R-10024); Curved Standard Ball Burr XL, 5.0mm (R-10025); Curved Shaver XL 4.2mm (R-10026); Curved Dynablator, XL (R-10027) (May 8, 2024)

Source page: https://510kreport.com/company/relign-subsidiary-of-zimmer-biomet