Prosthesis, Wrist, Hemi-, Ulnar
FDA product code KXE · Class 2 · 3 devices · 3 reports · 0 devices named in recalls
- NA DRUJ-IS145Aptis Medical, LLC · Prosthesis, Wrist, Hemi-, Ulnar1 report
- NA DRUJ-IS160Aptis Medical, LLC · Prosthesis, Wrist, Hemi-, Ulnar1 report
- NA DRUJ-LP10Aptis Medical, LLC · Prosthesis, Wrist, Hemi-, Ulnar1 report