Reliance Medical Systems, LLC
Sandy, UT, US
Reliance Medical Systems, LLC appears in FDA device records in Sandy, UT. FDA records list 27 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 27
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 27 510(k) clearances for Reliance Medical Systems, LLC between 2007 and 2022. The busiest year on record is 2012, with 5. The most recent is 2022, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 2007 | 1 |
| 2008 | 2 |
| 2009 | 1 |
| 2010 | 1 |
| 2012 | 5 |
| 2013 | 2 |
| 2014 | 1 |
| 2015 | 4 |
| 2016 | 2 |
| 2017 | 2 |
| 2018 | 2 |
| 2019 | 2 |
| 2021 | 1 |
| 2022 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K202266 | Reliance Cervical IBF System | ODP | Substantially Equivalent | |
| K210874 | Reliance Spinal Screw System | NKB | Substantially Equivalent | |
| K183049 | Reliance Lumbar IBF System | MAX | Substantially Equivalent | |
| K181118 | Reliance Lumbar IBF System | OVD | Substantially Equivalent | |
| K180687 | Reliance Lumber IBF System | MAX | Substantially Equivalent | |
| K173283 | Reliance Lumbar IBF System | MAX | Substantially Equivalent | |
| K173102 | Reliance Cervical IBF System | ODP | Substantially Equivalent | |
| K172489 | Reliance Cervical IBF System | ODP | Substantially Equivalent | |
| K162066 | Reliance Spinal Screw System | MNH | Substantially Equivalent | |
| K160463 | Reliance Lumbar IBF System | MAX | Substantially Equivalent | |
| K152131 | Reliance Spinal Screw System | MNI | Substantially Equivalent | |
| K142269 | Reliance Cervical IBF System | ODP | Substantially Equivalent | |
| K142867 | Reliance Posterior Cervical-Thoracic System | KWP | Substantially Equivalent | |
| K142217 | Reliance Interspinous Plate System | PEK | Substantially Equivalent | |
| K140742 | RELIANCE ANTERIOR CERVICAL PLATE | KWQ | Substantially Equivalent | |
| K131429 | RELIANCE CERVICAL IBF SYSTEM | ODP | Substantially Equivalent | |
| K123521 | RELIANCE SPINAL SCREW SYSTEM | MNI | Substantially Equivalent | |
| K122292 | RELIANCE POSTERIOR CERVICAL- THORACIC SYSTEM | KWP | Substantially Equivalent | |
| K122216 | RELIANCE ANTERIOR CERVICAL PLATE SYSTEM | KWQ | Substantially Equivalent | |
| K120396 | RELIANCE CERVICAL IBF SYSTEM | ODP | Substantially Equivalent | |
| K113540 | RELIANCE LUMBAR IBF SYSTEM | MAX | Substantially Equivalent | |
| K110896 | RELIANCE SPINAL SCREW SYSTEM | MNI | Substantially Equivalent | |
| K101112 | RELIANCE SPINAL SCREW SYSTEM | KWP | Substantially Equivalent | |
| K081978 | RELIANCE SPINAL SCREW SYSTEM | MNI | Substantially Equivalent | |
| K081383 | RELIANCE VBS SYSTEM | MQP | Substantially Equivalent | |
| K073349 | RELIANCE BUTTRESS WASHER SYSTEM | KWQ | Substantially Equivalent | |
| K063637 | RELIANCE VBS SYSTEM | MQP | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
- KWPAppliance, Fixation, Spinal Interlaminal
- KWQAppliance, Fixation, Spinal Intervertebral Body
- ODPIntervertebral Fusion Device With Bone Graft, Cervical
- MAXIntervertebral Fusion Device With Bone Graft, Lumbar
- OVDIntervertebral Fusion Device With Integrated Fixation, Lumbar
- MNIOrthosis, Spinal Pedicle Fixation
- MNHOrthosis, Spondylolisthesis Spinal Fixation
- MQPSpinal Vertebral Body Replacement Device
- PEKSpinous Process Plate
- NKBThoracolumbosacral Pedicle Screw System
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.
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Data as of , FDA export datePage updated Source: openFDA, public domain