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FDA 510(k)

GRIND NO MORE VERSION 2 AND 3

K-Number: K091175 · 2009-05-08

ApplicantRanir, LLC
Decision Date2009-05-08
Product CodeOBR
DecisionSubstantially Equivalent

Device Summary

GRIND NO MORE VERSION 2 AND 3 is the device name listed in this FDA 510(k) record. The listed applicant is Ranir, LLC. It received FDA 510(k) clearance on 2009-05-08 under 510(k) number K091175. The device is classified under product code OBR. Product code OBR falls under the category of Orthopedic, which includes orthopedic implants, fixation devices, and surgical instruments. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GRIND NO MORE VERSION 2 AND 3?

GRIND NO MORE VERSION 2 AND 3 is a medical device that received FDA 510(k) clearance on 2009-05-08. The listed applicant is Ranir, LLC. The 510(k) number is K091175.

When did GRIND NO MORE VERSION 2 AND 3 receive FDA 510(k) clearance?

GRIND NO MORE VERSION 2 AND 3 received FDA 510(k) clearance on 2009-05-08, under 510(k) number K091175.

Who is the listed applicant for GRIND NO MORE VERSION 2 AND 3?

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 GRIND NO MORE VERSION 2 AND 3?

The FDA product code for GRIND NO MORE VERSION 2 AND 3 is OBR. This falls under the Orthopedic category.

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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 PROTECTORK103004SNORE GUARDK102118SNORE GUARD ADVANCEK094020GRIND NO MORE GENERATION II

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Related Devices (Code: OBR)

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.

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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.

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