Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

SNORE GUARD

K-Number: K103004 · 2011-02-25

ApplicantRanir, LLC
Decision Date2011-02-25
Product CodeLRK
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

SNORE GUARD is the device name listed in this FDA 510(k) record. The listed applicant is Ranir, LLC. It received FDA 510(k) clearance on 2011-02-25 under 510(k) number K103004. The device is classified under product code LRK. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SNORE GUARD?

SNORE GUARD is a medical device that received FDA 510(k) clearance on 2011-02-25. The listed applicant is Ranir, LLC. The 510(k) number is K103004.

When did SNORE GUARD receive FDA 510(k) clearance?

SNORE GUARD received FDA 510(k) clearance on 2011-02-25, under 510(k) number K103004.

Who is the listed applicant for SNORE GUARD?

The FDA 510(k) record lists Ranir, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SNORE GUARD?

The FDA product code for SNORE GUARD is LRK.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Ranir, LLC as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K133423REST ASSURED EXTRA COMFORT NITE PROTECTORK120103REST ASSURED GENERATION III DENTAL PROTECTORK112879REST ASSURED READY TO WEAR NITE PROTECTORK102118SNORE GUARD ADVANCEK094020GRIND NO MORE GENERATION IIK091175GRIND NO MORE VERSION 2 AND 3

View all 8 devices →

Related Devices (Code: LRK)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K262104Anti Snoring Mouthpiece (L09-BB, L09-PP, L09-TB, L09-BT, L09-TP, L09-PT, L09-TT)Ram.Shaw Pte., Ltd.K261912SnØreNegatØrDnB Innovations, LLCK261366VirtusSomnomed, Inc.K261251Snorbliss® Anti-Snoring DeviceEndeavor Commerce, LLCK261134Dormiva Anti-Snoring Mouth GuardKoncept Innovators, Inc.K252942ShaeferHShaeferh, LLC

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑