Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Accelerated Rehab Designs, 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) |
|---|---|---|---|---|---|
| K012281 | TRS-2000 POWER TILT/POWER RECLINE SYSTEM | Accelerated Rehab Designs, Inc. | 2001-08-01 | 12 | 0 |
| K010011 | TE-2000 POWER TILT/POWER ELEVATING SEAT COMBINATION SYSTEM | Accelerated Rehab Designs, Inc. | 2001-01-12 | 10 | 0 |
| K992828 | E-2000 POWER ELEVATING SEAT SYSTEM, MODELS ARD-ESTORM, ARD-E | Accelerated Rehab Designs, Inc. | 2000-02-03 | 164 | 0 |
| K992804 | T-2000-POWER TILT SEATING SYSTEM, MODELS ARD-TSTORM, ARD-TP- | Accelerated Rehab Designs, Inc. | 2000-02-03 | 168 | 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