FDA 510(k)

Clench Relief Mouth Piece PRO RX, Clench Relief Mouth Piece

Número K: K222845 · 2023-11-28

Data da decisão2023-11-28

Código do produtoMQC

DecisãoSubstantially Equivalent

Resumo do dispositivo

Clench Relief Mouth Piece PRO RX, Clench Relief Mouth Piece is the device name listed in this FDA 510(k) record. The listed applicant is Frey Oral Technologies, LLC. It received FDA 510(k) clearance on 2023-11-28 under 510(k) number K222845. The device is classified under product code MQC. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Clench Relief Mouth Piece PRO RX, Clench Relief Mouth Piece?

Clench Relief Mouth Piece PRO RX, Clench Relief Mouth Piece is a medical device that received FDA 510(k) clearance on 2023-11-28. The listed applicant is Frey Oral Technologies, LLC. The 510(k) number is K222845.

When did Clench Relief Mouth Piece PRO RX, Clench Relief Mouth Piece receive FDA 510(k) clearance?

Clench Relief Mouth Piece PRO RX, Clench Relief Mouth Piece received FDA 510(k) clearance on 2023-11-28, under 510(k) number K222845.

Who is the listed applicant for Clench Relief Mouth Piece PRO RX, Clench Relief Mouth Piece?

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

What is the FDA product code for Clench Relief Mouth Piece PRO RX, Clench Relief Mouth Piece?

The FDA product code for Clench Relief Mouth Piece PRO RX, Clench Relief Mouth Piece is MQC.

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