Data / Medical devices / United States / Hill Laboratories
Hill Laboratories: FDA-registered device maker in Frazer, PA, United States, 15 510(k) clearances
Hill Laboratories is registered with the FDA (registration 2510425) in Frazer, PA, United States. It lists 9 device types. The FDA files 15 510(k) clearances under its listings, the newest dated June 20, 2018. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 2510425
- Address
- 3 N. Bacton Hill Rd., Frazer, PA, United States, 19355
- Owner or operator
- Hill Laboratories (10023824)
- Roles
- Manufacturer, Repackager or relabeler, Specification developer
- First device listed
- December 17, 2007
- Registered through
- 2026
- Brand names listed
- ACR Table, AFT, Air Drop AFT, Air Flex II, Air Flex II with Auto Distract, Atlas Percussion Adjusting Instrument, Model C-1000, Best Tec, Clarity Chair and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Apparatus, Traction, Non-Powered | HST | 1 | Manufacturer | accessdata.fda.gov |
| Equipment, Traction, Powered | ITH | 2 | Manufacturer | accessdata.fda.gov |
| Exerciser, Powered | BXB | 1 | Manufacturer | accessdata.fda.gov |
| Interferential Current Therapy | LIH | 2 | Repackager or relabeler | accessdata.fda.gov |
| Lamp, Infrared, Therapeutic Heating | ILY | 2 | Repackager or relabeler, Specification developer | accessdata.fda.gov |
| Manipulator, Plunger-Like Joint | LXM | U | Manufacturer | accessdata.fda.gov |
| Stationary Ultrasonic Diathermy Device For Use In Applying Therapeutic Deep Heat | PFW | 2 | Repackager or relabeler | accessdata.fda.gov |
| Table, Physical Therapy, Multi Function | JFB | 2 | Manufacturer | accessdata.fda.gov |
| Table, Powered | INQ | 1 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| June 20, 2018 | K172536 | Atlas Percussion Adjusting Instrument | LXM | Substantially Equivalent | Spinalight, Inc. | accessdata.fda.gov |
| February 11, 2010 | K090250 | ELECTRO-LIGHT THERAPY | ILY | Substantially Equivalent | Hill Laboratories Co. | accessdata.fda.gov |
| March 12, 2008 | K072256 | HF54 COMBINATION ULTRASOUND INTERFERENTIAL AND PREMODULATED STIMULATION SYSTEM WITH OPTIONAL HANDS-FREE OPERATION, MODEL | PFW | Substantially Equivalent | Hill Laboratories Co. | accessdata.fda.gov |
| December 14, 2006 | K063034 | AIR-FLEX WITH AUTO-DISTRACTION | JFB | Substantially Equivalent | Hill Laboratories Co. | accessdata.fda.gov |
| December 22, 2004 | K043239 | HEALTHSTAR ELITE | ITH | Substantially Equivalent | Hill Laboratories Co. | accessdata.fda.gov |
| July 6, 1995 | K952357 | THE HILL ADJUSTABLE PODIATRY MODEL | INQ | Substantially Equivalent | Hill Laboratories Co. | accessdata.fda.gov |
| June 22, 1995 | K952359 | THE HILL ADJUSTABLE HA90C | INQ | Substantially Equivalent | Hill Laboratories Co. | accessdata.fda.gov |
| June 22, 1995 | K952358 | THE HILL ADJUSTABLE P.T. MOBILIZATION TABLE | INQ | Substantially Equivalent | Hill Laboratories Co. | accessdata.fda.gov |
| June 22, 1995 | K952356 | THE HILL ADJUSTABLE COUNTERSTRAIN TABLE | INQ | Substantially Equivalent | Hill Laboratories Co. | accessdata.fda.gov |
| June 22, 1995 | K952355 | THE HILL ADJUSTABLE 90MD | INQ | Substantially Equivalent | Hill Laboratories Co. | accessdata.fda.gov |
| June 22, 1995 | K942109 | THE HILL ADJUSTABLE RATH MECHANICAL TABLE | INQ | Substantially Equivalent | Hill Laboratories Co. | accessdata.fda.gov |
| February 17, 1995 | K942026 | THE HILL ADJUSTABLE HA90E | INQ | Substantially Equivalent | Hill Laboratories Co. | accessdata.fda.gov |
| February 17, 1995 | K934754 | THE HILL HI-LO TABLE | INQ | Substantially Equivalent | Hill Laboratories Co. | accessdata.fda.gov |
| June 29, 1993 | K931832 | THE HILL ADJUSTABLE HA90 | INQ | Substantially Equivalent | Hill Laboratories Co. | accessdata.fda.gov |
| March 31, 1993 | K925271 | REPEX-REPEATED ENDRANGE PASSIVE EXERCISE MACHINE | BXB | Substantially Equivalent | Repex Intl., Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Table, Powered
- All makers of Lamp, Infrared, Therapeutic Heating
- All makers of Apparatus, Traction, Non-Powered
- All makers of Equipment, Traction, Powered
- All makers of Exerciser, Powered
- All makers of Stationary Ultrasonic Diathermy Device For Use In Applying Therapeutic Deep Heat
Updated June 20, 2018. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.