Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Benz Research and Development Corp. — Predicate Candidate Screening
12 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
115 daysmedian FDA review time
317 days90th percentile
12clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K101122 | BENZ-G 4X (HIOXIFILCON D) MULTIFOCAL LATHED LENS | Benz Research and Development Corp. | 2010-08-09 | 110 | 0 |
| K062854 | BENZ-G 4X HIOXIFILCON D | Benz Research and Development Corp. | 2007-08-06 | 315 | 0 |
| K003861 | BENZ-MF (VISIBILITY HANGLING TINT) (METHAFILCON A) SOFT DAIL | Benz Research and Development Corp. | 2001-03-08 | 85 | 0 |
| K992692 | EXTREME H20 (HIOXIFILICON A) SOFT CONTACT LENS | Benz Research and Development Corp. | 1999-10-18 | 68 | 0 |
| K983773 | BENZ G-5X (HIOXIFILCON A) SOFT DAILY WEAR CONTACT LENS | Benz Research and Development Corp. | 1998-12-22 | 57 | 0 |
| K980418 | BENZ METHAFILCON A OPTICAL BLANK, BENZ METHAFILCON A SPHERIC | Benz Research and Development Corp. | 1998-02-27 | 24 | 0 |
| K972807 | (LENSES)BENZ HEFILCON A SPHERICAL/TORIC SOFT (HYDROPHILIC) C | Benz Research and Development Corp. | 1997-10-15 | 79 | 0 |
| K963744 | BENZ B36 (KOLFOCON B) RIGID GAS PERMEABLE (HYDROPHOBIC) DAIL | Benz Research and Development Corp. | 1997-07-31 | 317 | 0 |
| K963512 | BENZ B17 (KOLFOCON A) RIGID GAS PERMEABLE (HYDROPHOBIC DAILY | Benz Research and Development Corp. | 1997-07-31 | 335 | 0 |
| K964528 | (LENSES) BENZ-G 3X (HIOXIFILCON B) SPHERICAL AND TORIC SOFT | Benz Research and Development Corp. | 1997-03-07 | 115 | 0 |
| K961103 | BENZ 38 CLEAR & WITH BLUE VISIBILITY TINT | Benz Research and Development Corp. | 1996-08-23 | 156 | 0 |
| K952620 | OPTICAL BLANKS: BENZ55G CLEAR AND VISIBILITY TINTED | Benz Research and Development Corp. | 1995-12-01 | 178 | 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