Dyonics, Inc.
Dyonics, Inc. holds FDA 510(k) medical device clearances, first cleared 1978, most recent 1990.
Top product codes for Dyonics, Inc.
Recent clearances by Dyonics, Inc.
- K900070 — MODIFIED USES OF THE ARTHROSCOPIC SURGICAL SYSTEM
- K896416 — DYONICS SHOULDER PORTAL SYSTEM
- K893136 — SURGI-PAK FOR ARTHROSCOPIC ACROMIOPLASTY
- K890665 — MODIFIED CANNULA, TROCAR AND OBTURATOR ACCESSORIES
- K894728 — DYONICS DISPOSABLE ARTHROSCOPIC SURGICAL KNIFE
- K892062 — PS3500 ARTHROSCOPIC SURGICAL SYSTEM
- K884839 — MODIFIED SAW BLADES TO THE SAGITAL SAW
- K881876 — DYNAMIC CRUCIATE TESTER
- K880739 — DYONICS DRILL GUIDE/ISOMETER SYSTEM
- K880150 — PACESETTER (TM) 3500 ARTHROSCOPIC SURGICAL SYSTEM
- K870212 — ARTHROSCOPIC SHOULDER HOLDER
- K862017 — ARTHROSCOPIC SHOULDER LIGAMENT REPAIR KIT
- K843121 — GUIDE TO THE KNEE
- K833943 — MENISCAL SUTURING SYSTEM
- K833587 — DISPOSABLE ARTHROSCOPY BLADE
- K820367 — INTRA-ARTICULAR SURGICAL SYSTEM
- K812506 — THE ARTHROFILE
- K790502 — DYONICS STEROTOXIC POSITIONER
- K771218 — INTRA-ARTICULAR SHAVER
Data sourced from openFDA. This site is unofficial and independent of the FDA.