Atlantis Components, Inc.
Atlantis Components, Inc. holds FDA 510(k) medical device clearances, first cleared 1999, most recent 2011.
Top product codes for Atlantis Components, Inc.
Recent clearances by Atlantis Components, Inc.
- K103020 — ATLANTIS ABUTMENT FOR KEYSTONE IMPLANT, ATLANTIS GEMINI ABUTMENT
- K073540 — ATLANTIS ABUTMENT IN ZIRCONIA FOR BIOHORIZONS IMPLANT
- K073258 — ATLANTIS ABUTMENT FOR BIOHORIZON IMPLANTS, ATLANTIS GEMINI ABUTMENT FOR BIOHORIZON IMPLANTS, ATLANTIS GEMINI + ABUTMENT
- K072483 — ATLANTIS ABUTMENT IN ZIRCONIA FOR 3I CERTAIN MICROAMINI IMPLANTS, GEMINI ABUTMENT IN ZIRCONIA FOR ASTRA IMPLANTS
- K071946 — ATLANTIS, GEMINI AND GEMINI+ ABUTMENTS IN ZIRCONIA FOR ASTRA IMPLANTS
- K070833 — ATLANTIS ABUTMENT FOR ASTRA IMPLANT
- K063734 — ATLANTIS ABUTMENT IN ZIRCONIA FOR 3I CERTAIN INTERFACE
- K062197 — ATLANTIS ABUTMENT FOR 3I CERTAIN MICRO MINI; GEMINI AND GEMINI+ ABUTMENT
- K062069 — ATLANTIS ABUTMENT FOR 3I MICROMINI IMPLANT
- K062277 — ATLANTIS ABUTMENT IN ZIRCONIA FOR NOBEL BIOCARE REPLACE
- K053654 — ATLANTIS ABUTMENT FOR NOBEL REPLACE INTERFACE
- K053373 — ATLANTIS ABUTMENT FOR ZIMMER INTERFACE
- K053450 — ATLANTIS ABUTMENT FOR ZIMMER INTERFACE
- K052070 — ATLANTIS ABUTMENT IN ZIRCONIA, ATLANTIS GEMINI ABUTMENT IN ZIRCONIA, ATLANTIS GEMEINI + ABUTMENT IN ZIRCONIA
- K051652 — ATLANTIS ABUTMENT, ATLANTIS GEMINI ABUTMENT, ATLANTIS GEMINI+ ABUTMENT
- K051011 — ENDOSSEOUS DENTAL IMPLANT ABUTMENT
- K050052 — ATLANTIS ABUTMENT FOR STRAUMANN INTERFACE
- K981858 — ATLANTIS ABUTMENT AND ATLANTIS ABUTMENT SCREW
Data sourced from openFDA. This site is unofficial and independent of the FDA.