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FDA 510(k)

GRIND NO MORE GENERATION II

K-Number: K094020 · 2010-01-25

ApplicantRanir, LLC
Decision Date2010-01-25
Product CodeOBR
DecisionSubstantially Equivalent

Device Summary

GRIND NO MORE GENERATION II is the device name listed in this FDA 510(k) record. The listed applicant is Ranir, LLC. It received FDA 510(k) clearance on 2010-01-25 under 510(k) number K094020. 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 GENERATION II?

GRIND NO MORE GENERATION II is a medical device that received FDA 510(k) clearance on 2010-01-25. The listed applicant is Ranir, LLC. The 510(k) number is K094020.

When did GRIND NO MORE GENERATION II receive FDA 510(k) clearance?

GRIND NO MORE GENERATION II received FDA 510(k) clearance on 2010-01-25, under 510(k) number K094020.

Who is the listed applicant for GRIND NO MORE GENERATION II?

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 GENERATION II?

The FDA product code for GRIND NO MORE GENERATION II 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 ADVANCEK091175GRIND NO MORE VERSION 2 AND 3

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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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