Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Inmark Corp. · Predicate Candidate Screening
4 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K910308 | X-RAY TUBE HOUSING ASSEMBLY POLARIX II GEN/XO 110 | Inmark Corp. | 1991-03-27 | 62 | 0 |
| K910276 | X-RAY TUBE HOUSING ASSEMBLY SOREDEX DC/CIR 51 | Inmark Corp. | 1991-03-06 | 42 | 0 |
| K894742 | RELOADING OF X-RAY TUBE HOUSING ASSEM., VARIOUS | Inmark Corp. | 1989-10-27 | 102 | 0 |
| K894413 | X-RAY TUBE HOUSING ASSEMBLY, VARIOUS MODELS | Inmark Corp. | 1989-09-22 | 67 | 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