Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Arbor Technologies, Inc. — Predicate Candidate Screening
10 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
234 daysmedian FDA review time
651 days90th percentile
10clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K960928 | SYRINGEFILTER | Arbor Technologies, Inc. | 1997-04-04 | 393 | 0 |
| K964283 | AUTOPRIME | Arbor Technologies, Inc. | 1997-01-22 | 86 | 0 |
| K922777 | PRESSURE TUBING AND ACCESSORIES | Arbor Technologies, Inc. | 1994-03-22 | 651 | 0 |
| K902666 | ANESTHESIA CONDUCTION FILTER | Arbor Technologies, Inc. | 1991-04-23 | 309 | 0 |
| K895859 | CONTAIN(TM) | Arbor Technologies, Inc. | 1991-02-07 | 492 | 0 |
| K902167 | CONTAIN(TM) LASER PLUME FILTER | Arbor Technologies, Inc. | 1991-01-04 | 234 | 0 |
| K890844 | MICROSEPT 60/20 | Arbor Technologies, Inc. | 1989-06-07 | 106 | 0 |
| K874505 | CONTAIN(TM) | Arbor Technologies, Inc. | 1988-05-20 | 200 | 0 |
| K864113 | CLYDE (TM) FILTRATION SYSTEM | Arbor Technologies, Inc. | 1987-02-04 | 106 | 0 |
| K863162 | VACU-GUARD | Arbor Technologies, Inc. | 1986-08-29 | 11 | 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