Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Caremed Supply, 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) |
|---|---|---|---|---|---|
| K181217 | VesoFlow Lite DVT Compression Device | Caremed Supply, Inc. | 2018-08-05 | 90 | 0 |
| K141064 | VESOFLOW PLUS DVT COMPRESSION DEVICE | Caremed Supply, Inc. | 2014-12-04 | 224 | 0 |
| K122873 | VASOPOUSE DEEP VEIN THROMBOSIS COMPRESSION DEVICE MODEL IPCS | Caremed Supply, Inc. | 2013-01-15 | 118 | 0 |
| K110977 | VESOFLOW | Caremed Supply, Inc. | 2011-08-25 | 140 | 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