Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Degussa Corp. — Predicate Candidate Screening
24 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
49 daysmedian FDA review time
66 days90th percentile
24clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K973288 | STABILOR HN | Degussa Corp. | 1997-11-19 | 78 | 0 |
| K972910 | PORS ON LITE | Degussa Corp. | 1997-10-14 | 68 | 0 |
| K960256 | DEGUDENT LS | Degussa Corp. | 1996-02-21 | 34 | 0 |
| K960226 | DG 88 | Degussa Corp. | 1996-02-14 | 28 | 0 |
| K960104 | BIOCCLUS 4 | Degussa Corp. | 1996-02-06 | 26 | 0 |
| K955465 | DEGUPRINT | Degussa Corp. | 1995-12-28 | 28 | 0 |
| K955118 | DEGUBOND X-LITE PLUS | Degussa Corp. | 1995-12-11 | 32 | 0 |
| K955027 | DEGUBOND X-LITE | Degussa Corp. | 1995-12-01 | 29 | 0 |
| K951789 | PALLIAG NF IV | Degussa Corp. | 1995-06-14 | 58 | 0 |
| K951788 | DEGULOR S | Degussa Corp. | 1995-06-12 | 56 | 0 |
| K951786 | DEGULOR A | Degussa Corp. | 1995-06-12 | 56 | 0 |
| K951790 | PONTALLOR 3 | Degussa Corp. | 1995-06-12 | 56 | 0 |
| K951791 | DEPALOR | Degussa Corp. | 1995-06-12 | 56 | 0 |
| K951787 | DEGUBOND 4 | Degussa Corp. | 1995-06-08 | 52 | 0 |
| K951785 | PRIMALLOR 2 | Degussa Corp. | 1995-06-06 | 50 | 0 |
| K951784 | PRIMALLOR 1 | Degussa Corp. | 1995-06-06 | 50 | 0 |
| K951783 | BOND-ON 4 | Degussa Corp. | 1995-06-02 | 46 | 0 |
| K951779 | DEGULOR M | Degussa Corp. | 1995-06-02 | 49 | 0 |
| K951781 | PORS ON PLUS | Degussa Corp. | 1995-06-02 | 49 | 0 |
| K951780 | STABILOR NF IV | Degussa Corp. | 1995-06-01 | 48 | 0 |
| K951782 | STABILOR G | Degussa Corp. | 1995-06-01 | 48 | 0 |
| K951777 | DEGUSTAR GA-2 | Degussa Corp. | 1995-05-31 | 44 | 0 |
| K951778 | DEGUDENT U | Degussa Corp. | 1995-05-31 | 47 | 0 |
| K950187 | FUTURA ONE | Degussa Corp. | 1995-03-24 | 66 | 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