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FDA 510(k)

REST ASSURED READY TO WEAR NITE PROTECTOR

K-Number: K112879 · 2012-01-27

ApplicantRanir, LLC
Decision Date2012-01-27
Product CodeOBR
DecisionSubstantially Equivalent

Device Summary

REST ASSURED READY TO WEAR NITE PROTECTOR is the device name listed in this FDA 510(k) record. The listed applicant is Ranir, LLC. It received FDA 510(k) clearance on 2012-01-27 under 510(k) number K112879. 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 REST ASSURED READY TO WEAR NITE PROTECTOR?

REST ASSURED READY TO WEAR NITE PROTECTOR is a medical device that received FDA 510(k) clearance on 2012-01-27. The listed applicant is Ranir, LLC. The 510(k) number is K112879.

When did REST ASSURED READY TO WEAR NITE PROTECTOR receive FDA 510(k) clearance?

REST ASSURED READY TO WEAR NITE PROTECTOR received FDA 510(k) clearance on 2012-01-27, under 510(k) number K112879.

Who is the listed applicant for REST ASSURED READY TO WEAR NITE PROTECTOR?

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 REST ASSURED READY TO WEAR NITE PROTECTOR?

The FDA product code for REST ASSURED READY TO WEAR NITE PROTECTOR is OBR. This falls under the Orthopedic category.

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.

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.

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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.

Official Source

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

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