Dacomed Corp.
FDA 510(k) medical device clearances.
Top product codes for Dacomed Corp.
Recent clearances by Dacomed Corp.
- K953640 — DUNA II PENILE PROSTHESIS
- K941781 — RIGISCAN PLUS RIGIDITY ASSESSMENT SYSTEM
- K920409 — DACOMED BATTERY OPERATED VACUUM ERECTION DEVICE
- K920420 — DURA II PENILE PROSTHESIS
- K912344 — MODIFIED DURAPHASE(TM) IMPLANTED PENILE PROSTHESIS
- K900774 — DACOMED NEGATIVE PRESSURE ERECTION DEVICE
- K885323 — DACOMED EXTERNAL MALE CONTINENCE DEVICE
- K880391 — DACOMED CYSTOMETER
- K871653 — DURAPHASE PENILE PROSTHESIS
- K870320 — DACOMED PENILE PROSTHESIS SIZER
- K854118 — DACOMED CORP. ESKA-HERRMAN VOICE PROSTHESIS
- K850019 — OMNI PHASE PENILE PROSTHESIS
- K843186 — ESKA MULTISTAGE ESOPHAGEAL BOUGIE
- K841202 — DACOMED RIGISCAN SYSTEM
- K834504 — ESKA JONAS SILICON-SILVER PENILE
- K830667 — SILICONE-SILVER PENILE PROSTHESIS-ESK
- K832121 — DACOMED SNAP-GAUGE
- K820615 — DACOMED SNAP-GAUGE
- K820081 — ESKA JONAS SILICONE-SILVER PENILE PROST
- K811693 — FORDER RETRACTOR
Data sourced from openFDA. This site is unofficial and independent of the FDA.