Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Lares Research, Inc. · Predicate Candidate Screening
8 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
90 daysmedian FDA review time
182 days90th percentile
8clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K141221 | LARES ULTRALITE PROSTYLE HIGH-SPEED DENTAL HANDPIECES, LARES | Lares Research, Inc. | 2014-10-28 | 169 | 0 |
| K031540 | APEX ELECTRIC HANDPIECE SYSTEM | Lares Research, Inc. | 2003-06-30 | 45 | 0 |
| K011960 | LARES RESEARCH SUNLASE 800P LASER SYSTEM (TO BE SOLD AS POCK | Lares Research, Inc. | 2001-12-21 | 182 | 0 |
| K983524 | LARES RESEARCH SUNLASE 800P LASER SYSTEM (TO BE SOLD AS PEIO | Lares Research, Inc. | 1999-04-01 | 175 | 0 |
| K961163 | LARES RESEARCH AS-1 LOWSPEED HANDPIECE | Lares Research, Inc. | 1996-04-23 | 32 | 0 |
| K905542 | LARES APOLLO CS AND S HANDPIECE LIGHTING SYSTEMS | Lares Research, Inc. | 1991-03-11 | 90 | 0 |
| K905543 | LARES APOLLO CS/CP/C | Lares Research, Inc. | 1991-03-11 | 90 | 0 |
| K905541 | LARES 757 WORKHORSE HIGHSPEED HANDPIECE | Lares Research, Inc. | 1991-03-07 | 86 | 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