Data / Medical devices / United States / Links Medical Products, Inc.
Links Medical Products, Inc.: FDA-registered device maker in Scottsdale, AZ, United States, 4 510(k) clearances
Links Medical Products, Inc. is registered with the FDA (registration 3027529701) in Scottsdale, AZ, United States. It lists 4 device types. The FDA files 4 510(k) clearances under its listings, the newest dated October 28, 2022. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3027529701
- Address
- 15979 N 76th Street, Suite D --, Scottsdale, AZ, United States, 85260
- Owner or operator
- LINKS MEDICAL PRODUCTS, INC. (9040995)
- Roles
- Repackager or relabeler, Specification developer
- First device listed
- April 6, 2000
- Registered through
- 2026
- Brand names listed
- LMP Diagnostics, Pill Crushing Pouch, Silent Knight, Silent Knight Pill Crushing Pouch, Silent Knight Pill Crushing Pouch (NONPC-1001)
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Container, Liquid Medication, Graduated | KYW | 1 | Specification developer | accessdata.fda.gov |
| Dressing, Wound, Drug | FRO | U | Specification developer | accessdata.fda.gov |
| Pill Crusher/Cutter | OHY | 1 | Repackager or relabeler | accessdata.fda.gov |
| Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature | FMK | 2 | Repackager or relabeler | 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 |
|---|---|---|---|---|---|---|
| October 28, 2022 | K221521 | Disposable Safety Lancet | FMK | Substantially Equivalent | SteriLance Medical (Suzhou), Inc. | accessdata.fda.gov |
| May 2, 2014 | K133934 | MANUKA FOAM HC, MANUKA FOAM HC (WITH ACRYLIC ADHESIVE BORDER), MANUKA FOAM HC (WITH SILICONE ADHESIVE BORDER) | FRO | Substantially Equivalent | Links Medical Products, Inc. | accessdata.fda.gov |
| March 14, 2014 | K131796 | MANUKA FILL WOUND DRESSING | FRO | Substantially Equivalent | Links Medical Products, Inc. | accessdata.fda.gov |
| May 23, 2012 | K120976 | MANUKA IG | FRO | Substantially Equivalent | Links Medical Products, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Container, Liquid Medication, Graduated
- All makers of Pill Crusher/Cutter
- All makers of Dressing, Wound, Drug
- All makers of Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature
Updated October 28, 2022. 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.