Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
J. Aderer, Inc. — Predicate Candidate Screening
24 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
26 daysmedian FDA review time
47 days90th percentile
24clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K822957 | PURCAST | J. Aderer, Inc. | 1982-10-26 | 21 | 0 |
| K822956 | G CAST | J. Aderer, Inc. | 1982-10-26 | 21 | 0 |
| K821798 | 82 ALLOY | J. Aderer, Inc. | 1982-07-13 | 25 | 0 |
| K821832 | DEGUCAST U | J. Aderer, Inc. | 1982-07-06 | 14 | 0 |
| K821590 | PORS-ON | J. Aderer, Inc. | 1982-06-14 | 13 | 0 |
| K821572 | DUALLOR 'R' | J. Aderer, Inc. | 1982-06-14 | 18 | 0 |
| K821407 | DEVA M | J. Aderer, Inc. | 1982-06-09 | 29 | 0 |
| K821521 | STABILOR NF | J. Aderer, Inc. | 1982-06-09 | 19 | 0 |
| K821446 | DEGUDENT 14 | J. Aderer, Inc. | 1982-06-09 | 26 | 0 |
| K821613 | E.G. BRIDGE GOLD | J. Aderer, Inc. | 1982-06-04 | 2 | 0 |
| K821299 | CER-MATE | J. Aderer, Inc. | 1982-05-28 | 24 | 0 |
| K821022 | PRECIOUS METAL ALLOYS | J. Aderer, Inc. | 1982-05-10 | 27 | 0 |
| K820955 | BOND-ON | J. Aderer, Inc. | 1982-05-05 | 29 | 0 |
| K820318 | SPECIAL WHITE | J. Aderer, Inc. | 1982-03-02 | 25 | 0 |
| K813418 | INZOMA NP | J. Aderer, Inc. | 1982-01-07 | 31 | 0 |
| K813417 | INZOMA P | J. Aderer, Inc. | 1982-01-07 | 31 | 0 |
| K811867 | SR-ALGICAP | J. Aderer, Inc. | 1981-10-02 | 93 | 0 |
| K811665 | SR-ISOCETTE | J. Aderer, Inc. | 1981-07-15 | 30 | 0 |
| K810686 | SR-IVOLEN | J. Aderer, Inc. | 1981-04-14 | 32 | 0 |
| K810687 | SR-IVOCAP | J. Aderer, Inc. | 1981-04-14 | 32 | 0 |
| K810523 | SR-IVOSEAL | J. Aderer, Inc. | 1981-04-14 | 47 | 0 |
| K810656 | SR-IVOSEAL(SOFT RELINING) | J. Aderer, Inc. | 1981-04-14 | 47 | 0 |
| K810524 | SR-IVOTRAY SPECIAL | J. Aderer, Inc. | 1981-03-17 | 19 | 0 |
| K810525 | SR-IVOTRAY UNIVERSAL | J. Aderer, Inc. | 1981-03-17 | 19 | 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