Planmeca Oy
Planmeca Oy holds FDA 510(k) medical device clearances, first cleared 1993, most recent 2023.
Top product codes for Planmeca Oy
Recent clearances by Planmeca Oy
- K230985 — Planmeca Viso
- K200572 — Planmeca Romexis
- K181576 — Planmeca Viso
- K171385 — Planmeca Romexis
- K160506 — Planmeca ProMax 3D Max, Planmeca Maximity
- K140713 — PLANMECA ROMEXIS
- K103689 — PLANMECA PROMAX 3D MID
- K093590 — PLANMECA PROMAX 3D MAX
- K091197 — PLANMECA PROSENSOR
- K072244 — PLANMECA PROONE
- K060328 — PLANMECA PROMAX 3D
- K051464 — PLANMECA PROMAX WITH DEC (DYNAMIC EXPOSURE CONTROL)
- K011619 — PROMAX, PANORAMIC X-RAY UNIT WITH CEPHALOSTAT
- K000771 — DIMAX 2
- K000428 — DIXI 2
- K000163 — PM 2002 PROLINE/AEC
- K000454 — DIMEX 2
- K984013 — PLANMECA INTRACAM STATION
- K980581 — PLANMECA DIXI, DIGITAL INTRAORAL X-RAY IMAGING SYSTEM
- K970812 — PM 2002 CC PROLINE
- K972033 — PLANMECA INTRACAM
- K970975 — PROSTYLE INTRA
- K970263 — PM 2002 CC PROLINE
- K963209 — PROSTYLE COMPACT
- K961420 — PROSTYLE COMPACT
- K955429 — PROSTYLE INTRA
- K952763 — PANORAMIC X-RAY UNIT (MODIFICATION)
- K934063 — PANORAMIC X-RAY UNITS, MODIFICATION
Data sourced from openFDA. This site is unofficial and independent of the FDA.