Atlantis Components, Inc.
Skokie, IL, US
Atlantis Components, Inc. appears in FDA device records in Skokie, IL. FDA records list 18 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 18
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 18 510(k) clearances for Atlantis Components, Inc. between 1999 and 2011. The busiest year on record is 2007, with 6. The most recent is 2011, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1999 | 1 |
| 2005 | 4 |
| 2006 | 4 |
| 2007 | 6 |
| 2008 | 2 |
| 2011 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K103020 | ATLANTIS ABUTMENT FOR KEYSTONE IMPLANT, ATLANTIS GEMINI ABUTMENT | NHA | Substantially Equivalent | |
| K073540 | ATLANTIS ABUTMENT IN ZIRCONIA FOR BIOHORIZONS IMPLANT | NHA | Substantially Equivalent | |
| K073258 | ATLANTIS ABUTMENT FOR BIOHORIZON IMPLANTS, ATLANTIS GEMINI ABUTMENT FOR BIOHORIZON IMPLANTS, ATLANTIS GEMINI + ABUTMENT | NHA | Substantially Equivalent | |
| K072483 | ATLANTIS ABUTMENT IN ZIRCONIA FOR 3I CERTAIN MICROAMINI IMPLANTS, GEMINI ABUTMENT IN ZIRCONIA FOR ASTRA IMPLANTS | NHA | Substantially Equivalent | |
| K071946 | ATLANTIS, GEMINI AND GEMINI+ ABUTMENTS IN ZIRCONIA FOR ASTRA IMPLANTS | NHA | Substantially Equivalent | |
| K070833 | ATLANTIS ABUTMENT FOR ASTRA IMPLANT | NHA | Substantially Equivalent | |
| K063734 | ATLANTIS ABUTMENT IN ZIRCONIA FOR 3I CERTAIN INTERFACE | NHA | Substantially Equivalent | |
| K062197 | ATLANTIS ABUTMENT FOR 3I CERTAIN MICRO MINI; GEMINI AND GEMINI+ ABUTMENT | NHA | Substantially Equivalent | |
| K062069 | ATLANTIS ABUTMENT FOR 3I MICROMINI IMPLANT | NHA | Substantially Equivalent | |
| K062277 | ATLANTIS ABUTMENT IN ZIRCONIA FOR NOBEL BIOCARE REPLACE | NHA | Substantially Equivalent | |
| K053654 | ATLANTIS ABUTMENT FOR NOBEL REPLACE INTERFACE | NHA | Substantially Equivalent | |
| K053373 | ATLANTIS ABUTMENT FOR ZIMMER INTERFACE | NHA | Substantially Equivalent | |
| K053450 | ATLANTIS ABUTMENT FOR ZIMMER INTERFACE | NHA | Substantially Equivalent | |
| K052070 | ATLANTIS ABUTMENT IN ZIRCONIA, ATLANTIS GEMINI ABUTMENT IN ZIRCONIA, ATLANTIS GEMEINI + ABUTMENT IN ZIRCONIA | NHA | Substantially Equivalent | |
| K051652 | ATLANTIS ABUTMENT, ATLANTIS GEMINI ABUTMENT, ATLANTIS GEMINI+ ABUTMENT | NHA | Substantially Equivalent | |
| K051011 | ENDOSSEOUS DENTAL IMPLANT ABUTMENT | NHA | Substantially Equivalent | |
| K050052 | ATLANTIS ABUTMENT FOR STRAUMANN INTERFACE | NHA | Substantially Equivalent | |
| K981858 | ATLANTIS ABUTMENT AND ATLANTIS ABUTMENT SCREW | DZE | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
There is no verification record for this company. Most companies on this site have none: a record exists only where a company asked to be verified and MDM ran the checks, so the absence of one says nothing about the company.
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Data as of , FDA export datePage updated Source: openFDA, public domain