Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Hill Laboratories Co. — Predicate Candidate Screening
17 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
206 daysmedian FDA review time
501 days90th percentile
17clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K090250 | ELECTRO-LIGHT THERAPY | Hill Laboratories Co. | 2010-02-11 | 374 | 0 |
| K083183 | AKLARUS PHOTOTHERAPY SYSTEM | Hill Laboratories Co. | 2009-07-16 | 261 | 0 |
| K072256 | HF54 COMBINATION ULTRASOUND INTERFERENTIAL AND PREMODULATED | Hill Laboratories Co. | 2008-03-12 | 212 | 0 |
| K062256 | HF54 COMBINATION ULTRASOUND INTERFERENTIAL AND PREMODULATED | Hill Laboratories Co. | 2007-02-26 | 206 | 0 |
| K063034 | AIR-FLEX WITH AUTO-DISTRACTION | Hill Laboratories Co. | 2006-12-14 | 72 | 0 |
| K043239 | HEALTHSTAR ELITE | Hill Laboratories Co. | 2004-12-22 | 29 | 0 |
| K952357 | THE HILL ADJUSTABLE PODIATRY MODEL | Hill Laboratories Co. | 1995-07-06 | 70 | 0 |
| K952358 | THE HILL ADJUSTABLE P.T. MOBILIZATION TABLE | Hill Laboratories Co. | 1995-06-22 | 56 | 0 |
| K952356 | THE HILL ADJUSTABLE COUNTERSTRAIN TABLE | Hill Laboratories Co. | 1995-06-22 | 52 | 0 |
| K952359 | THE HILL ADJUSTABLE HA90C | Hill Laboratories Co. | 1995-06-22 | 56 | 0 |
| K952355 | THE HILL ADJUSTABLE 90MD | Hill Laboratories Co. | 1995-06-22 | 56 | 0 |
| K942109 | THE HILL ADJUSTABLE RATH MECHANICAL TABLE | Hill Laboratories Co. | 1995-06-22 | 416 | 0 |
| K942256 | THE HILL ADJUSTABLE EXTEND-R TABLE | Hill Laboratories Co. | 1995-06-22 | 409 | 0 |
| K934754 | THE HILL HI-LO TABLE | Hill Laboratories Co. | 1995-02-17 | 501 | 0 |
| K932810 | THE HILL ADJUSTABLE AIR-FLEX MODEL | Hill Laboratories Co. | 1995-02-17 | 618 | 0 |
| K942026 | THE HILL ADJUSTABLE HA90E | Hill Laboratories Co. | 1995-02-17 | 297 | 0 |
| K931832 | THE HILL ADJUSTABLE HA90 | Hill Laboratories Co. | 1993-06-29 | 81 | 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