Smith & Nephew Dyonics, Inc.
FDA 510(k) medical device clearances.
Top product codes for Smith & Nephew Dyonics, Inc.
Recent clearances by Smith & Nephew Dyonics, Inc.
- K955914 — LIMITED REUSE ARTHROSCOPIC BLADES
- K954627 — ECTRA II LIGAMENT RELEASE SYSTEM
- K954989 — DYONICS DISPOSABLE ENDOSCOPIC SURGERY BLADES
- K953695 — DYONICS DISPOSABLE ARTHROSCOPIC BLADES
- K953387 — ECTRA LIGAMENT RELEASE SYSTEM
- K945182 — DYONICS FIXATION SCREWS
- K936071 — SMITH & NEPHEW DYONICS INC. ELECTRONIC ENDOSCOPE
- K934299 — DYONICS DISPOSABLE ARTHROSCOPIC SURGERY BLADES MODIFICATION
- K920267 — DYONICS ARTHROSCOPIC KIT
- K922176 — INTELIJET SUCTION SUPPLY
- K914963 — SMITH & NEPHEW DYONICS TMJ ARTHROSCOPY INFLOW SET
- K913401 — SUCTION CONTROL FOOTSWITCH WITH SPEED CONTROL
- K914559 — SMALL JOINT SYSTEM
- K914919 — SMITH & NEPHEW DYONICS LAPAROSCOPY SYSTEM
- K913347 — PALMER ARCH SUPPRESSOR
- K912453 — INTELIJET TM FLUID MANAGEMENT SYSTEM
- K904284 — ARTHROSCOPIC SURGICAL BLADE
- K903620 — MODIFIED ENDOSCOPIC CARPAL TUNNEL RELEASE SYSTEM
- K903193 — SMITH & NEPHEW DYONICS LEVELERT SYSTEM
- K901765 — POSTEROMEDIAL GUIDE
- K901616 — CANNULATED INTERFERENCE SCREW SYSTEM
- K901505 — ARTHROSCOPIC ELECTROSURGICAL PROBE
Data sourced from openFDA. This site is unofficial and independent of the FDA.