Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Core-Vent Corp. — Predicate Candidate Screening
25 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
165 daysmedian FDA review time
399 days90th percentile
25clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K002614 | ADVENT IMPLANT SYSTEM | Core-Vent Corp. | 2000-12-08 | 108 | 0 |
| K002188 | SWISSPLUS IMPLANT SYSTEM, MODEL SPWB 8,10,12,14/OPH20/SMPR, | Core-Vent Corp. | 2000-10-30 | 102 | 0 |
| K950576 | BIO-VENT X IMPLANT | Core-Vent Corp. | 1995-07-11 | 165 | 0 |
| K950577 | SWEDE-VENT IMPLANT | Core-Vent Corp. | 1995-07-11 | 165 | 0 |
| K950579 | MICRO-VENT IMPLANT | Core-Vent Corp. | 1995-07-11 | 165 | 0 |
| K950575 | BIO-VENT IMPLANT | Core-Vent Corp. | 1995-07-11 | 165 | 0 |
| K950578 | SCREW-VENT IMPLANT | Core-Vent Corp. | 1995-07-11 | 165 | 0 |
| K912059 | PRE-ANGLED ABUTMENTS | Core-Vent Corp. | 1992-02-11 | 278 | 0 |
| K913782 | TCAL ABUTMENT | Core-Vent Corp. | 1991-10-30 | 75 | 0 |
| K910585 | TSIR ANGLED ABUTMENTS | Core-Vent Corp. | 1991-10-04 | 235 | 0 |
| K902968 | BIO-VENT-X ENDOSSEOUS HA COATED DENTAL IMPLANTS | Core-Vent Corp. | 1991-05-15 | 313 | 0 |
| K900181 | MICRO-VENT ENDOSSEOUS IMPLANT ABUTMENTS | Core-Vent Corp. | 1991-02-20 | 400 | 0 |
| K900179 | SCREW-VENT ENDOSSEOUS IMPLANT ABUTMENTS | Core-Vent Corp. | 1991-02-20 | 400 | 0 |
| K900180 | CORE-VENT ENDOSSEOUS IMPLANT ABUTMENTS | Core-Vent Corp. | 1991-02-19 | 399 | 0 |
| K902969 | SCREW-VENT ENDOSSEOUS HA COATED DENTAL IMPLANTS | Core-Vent Corp. | 1990-12-17 | 164 | 0 |
| K900634 | SWEDE-VENT ENDOSSEOUS HA COATED DENTAL IMPLANTS | Core-Vent Corp. | 1990-11-09 | 273 | 0 |
| K900182 | SWEDE-VENT ENDOSSEOUS IMPLANT ABUTMENTS | Core-Vent Corp. | 1990-11-09 | 297 | 0 |
| K900177 | CORE-VENT ARMENTARIUM | Core-Vent Corp. | 1990-06-28 | 163 | 0 |
| K900178 | ELECTRIC MOTOR W/PHYSIO DISPENSER, HANDPIECES | Core-Vent Corp. | 1990-05-31 | 135 | 0 |
| K883717 | BIO-VENT | Core-Vent Corp. | 1989-09-01 | 367 | 0 |
| K873255 | THE MICRO-VENT/HA | Core-Vent Corp. | 1988-03-14 | 210 | 0 |
| K873818 | VENT CORP PIB IMPLANT | Core-Vent Corp. | 1988-02-26 | 162 | 0 |
| K864321 | MICRO-VENT | Core-Vent Corp. | 1987-01-07 | 65 | 0 |
| K861425 | SUB-VENT (TM) IMPLANT/ENDOSSEOUS BLADE IMPLANT | Core-Vent Corp. | 1986-11-05 | 203 | 0 |
| K861426 | SCREW-VENT (TM) IMPLANT/ENDOSSEOUS SCREW IMPLANT | Core-Vent Corp. | 1986-10-07 | 174 | 0 |
Methodology
Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.
Prepared with Atlas
Predicate research, review-time statistics and recall monitoring for 510(k) teams — atlasbyauro.com/fda