Medron, LLC
Salt Lake City, UT, US
MEDRON, LLC appears in FDA device records in Salt Lake City, UT. FDA records list 3 510(k) clearances between and , no PMA records and one registered establishment. As of , FDA records show no recalls for this company, and at least one establishment registration is current.
FDA records held for this company
510(k) clearance history
FDA records hold 3 510(k) clearances for Medron, LLC between 1994 and 2020. The busiest year on record is 1994, with 1. The most recent is 2020, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1994 | 1 |
| 1997 | 1 |
| 2020 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K192283 | MEDRON Vessel Dilator - 6F x 22cm HDPE Dilator, MEDRON Vessel Dilator - 15.5F - 17.5F HDPE Dilator | DRE | Substantially Equivalent | |
| K971897 | CONTINUOUS ARTERIOVENOUS HEMOFILTRATION CATHETER 10 FR (CAVH) | LFK | Substantially Equivalent | |
| K940775 | INJECTION CAP | FOZ | Substantially Equivalent |
Registered establishments
| Registration | FEI | Establishment | Address | Registration expires | Product codes listed |
|---|---|---|---|---|---|
| 1722746 | 1000306216 | MEDRON, LLC | 1518 S Gladiola St, SALT LAKE CITY, UT 84104 US | 2026 | and 13 more, listed in full below |
Registration numbers link to the FDA registration and listing record for that establishment.
FDA product codes
- KCJApplicator, Ent
- DQRCannula, Catheter
- PDUCatheter For Crossing Total Occlusions
- DWFCatheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
- LFKCatheter, Femoral
- MSDCatheter, Hemodialysis, Implanted
- MPBCatheter, Hemodialysis, Non-Implanted
- LJSCatheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days
- FOZCatheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
- DQYCatheter, Percutaneous
- LFJCatheter, Subclavian
- CAICircuit, Breathing (W Connector, Adaptor, Y Piece)
- FKADilator, Vessel
- DREDilator, Vessel, For Percutaneous Catheterization
- FBKEndoscopic Injection Needle, Gastroenterology-Urology
- OCXEndoscopic Irrigation/Suction System
- DTKFilter, Intravascular, Cardiovascular
- KNWInstrument, Biopsy
- DYBIntroducer, Catheter
- NFKKit, Repair, Catheter, Hemodialysis
- PNDMidline Catheter
- FEQPump, Air, Non-Manual, For Endoscope
- LKKPump, Infusion, Implanted, Programmable
- JXGShunt, Central Nervous System And Components
Recall records
No recall records for this company in the ingested FDA data.
Verification record
There is no verification record for this company. Most companies on this site have none: a record exists only where a company asked to be verified and MDM ran the checks, so the absence of one says nothing about the company.
Where there is a record, this is where it appears: what was checked, when it was checked, and the current status. An MDM Verified badge on another website links to a verify address on this domain that resolves to this section. A badge that does not resolve here is not ours.
MDM coverage
MDM coverage of this company lists here, newest first. Submit news.
Is this your company?
This page is built from public FDA records. Company pages are free and factual, and stay free whether or not anyone claims them. Membership never changes editorial coverage or vetting outcomes.
Claiming lets Medron, LLC edit what it says about itself and list the categories it works in. It grants no badge: claiming is not verification.
Data as of , FDA export datePage updated Source: openFDA, public domain