Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
International Medical Devices, Inc. · 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) |
|---|---|---|---|---|---|
| K223051 | Pre-Formed Silicone Block | International Medical Devices, Inc. | 2023-02-03 | 127 | 0 |
| K220760 | Pre-Formed Penile Silicone Block | International Medical Devices, Inc. | 2022-05-13 | 59 | 0 |
| K181387 | Pre-Formed Penile Silicone Block | International Medical Devices, Inc. | 2019-01-23 | 243 | 0 |
| K162624 | Pre-Formed Penile Silicone Block | International Medical Devices, Inc. | 2017-02-01 | 134 | 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