Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Ferris Mfg. Corp. — Predicate Candidate Screening
20 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
83 daysmedian FDA review time
356 days90th percentile
20clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K031660 | FERRIS POLYMEM STERILE BREAST PAD | Ferris Mfg. Corp. | 2005-02-22 | 636 | 0 |
| K031307 | FERRIS POLYMEM SILVER WOUND DRESSING | Ferris Mfg. Corp. | 2003-10-22 | 181 | 0 |
| K002129 | FERRIS POLYMEM STERILE WOUND DRESSING WITH COLLAGEN | Ferris Mfg. Corp. | 2000-08-25 | 42 | 0 |
| K991729 | FERRIS POLYOSTOMY STERILE WOUND DRESSING | Ferris Mfg. Corp. | 1999-08-27 | 99 | 0 |
| K990906 | FERRIS POLYMEM POLYWIC STERILE CAVITY WOUND FILLER | Ferris Mfg. Corp. | 1999-04-29 | 42 | 0 |
| K984539 | FERRIS POLYMEM CALCIUM ALGINATE STERILE WOUND DRESSING | Ferris Mfg. Corp. | 1999-03-01 | 70 | 0 |
| K982306 | POLYTUBE | Ferris Mfg. Corp. | 1998-09-22 | 83 | 0 |
| K932913 | FERRIS POLYMEM HYDROPHILIC WOUND DRESSING | Ferris Mfg. Corp. | 1994-06-07 | 356 | 0 |
| K900127 | FERRIS HYDROPHILIC DRESSING (ADD'L INDICATIONS) | Ferris Mfg. Corp. | 1990-05-18 | 129 | 0 |
| K880330 | FERRIS HYDROPHILIC DRESSING | Ferris Mfg. Corp. | 1988-03-23 | 56 | 0 |
| K874478 | DYNAFILM | Ferris Mfg. Corp. | 1988-01-14 | 73 | 0 |
| K873682 | FERRIS ECG ELECTRODE W/HYDROGEL | Ferris Mfg. Corp. | 1987-12-29 | 106 | 0 |
| K871675 | FERRIS TRANSPARENT WOUND DRESSING W/HYDROCOLLOID | Ferris Mfg. Corp. | 1987-08-06 | 100 | 0 |
| K872574 | TENSAGAIN | Ferris Mfg. Corp. | 1987-07-23 | 23 | 0 |
| K865089 | FERRIS DYNADERM PLUS | Ferris Mfg. Corp. | 1987-02-04 | 36 | 0 |
| K852375 | I.V. STARTER TRAY W/DYNADERM TRANSPARENT ADHESIVE | Ferris Mfg. Corp. | 1985-07-11 | 37 | 0 |
| K840152 | FERRIS VENT-A-DERM | Ferris Mfg. Corp. | 1984-08-30 | 230 | 0 |
| K790305 | ELECTRODES, FERRIS ECG, TYPES 905,906 | Ferris Mfg. Corp. | 1979-04-03 | 49 | 0 |
| K781371 | BONE MARROW ASPIRATION KIT | Ferris Mfg. Corp. | 1978-09-20 | 43 | 0 |
| K780784 | ASPIRATION NEEDLE | Ferris Mfg. Corp. | 1978-08-14 | 94 | 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