FDA 510(k)

Owl Night Guard

Numéro K : K253641 · 2026-02-26

Date de décision2026-02-26

Code produitOBR

DécisionSubstantially Equivalent

Résumé du dispositif

Owl Night Guard is the device name listed in this FDA 510(k) record. The listed applicant is Owl Dental Lab, Inc.. It received FDA 510(k) clearance on 2026-02-26 under 510(k) number K253641. 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.

Questions fréquentes

What is the Owl Night Guard?

Owl Night Guard is a medical device that received FDA 510(k) clearance on 2026-02-26. The listed applicant is Owl Dental Lab, Inc.. The 510(k) number is K253641.

When did Owl Night Guard receive FDA 510(k) clearance?

Owl Night Guard received FDA 510(k) clearance on 2026-02-26, under 510(k) number K253641.

Who is the listed applicant for Owl Night Guard?

The FDA 510(k) record lists Owl Dental Lab, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Owl Night Guard?

The FDA product code for Owl Night Guard is OBR. This falls under the Orthopedic category.

Essais cliniques associés

Les enregistrements connexes sont mis en correspondance automatiquement à l'aide des noms, codes produits ou autres métadonnées. Une mise en correspondance n'établit pas de relation clinique, scientifique, corporative ou réglementaire vérifiée ; veuillez consulter les sources officielles liées.

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Dispositifs connexes (Code : OBR)

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Source officielle

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