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GrindRelief PRO

FDA UDI

Class U (US FDA UDI)

by Grind Guard Technologies, L.L.C.

Identity

Trade Name
GrindRelief PRO FDA UDI
Generic Name
Mouthguard, reusable FDA UDI
Device Name
Thermoplastic mouth guard - Case of 3 FDA UDI
Model / Reference
203 FDA UDI
Description
Thermoplastic mouth guard - Case of 3 FDA UDI

Identifiers

Catalog Number
203 FDA UDI
Primary DI / UDI-DI
00866618000050 FDA UDI
510(k) Number
K133037 FDA UDI
FDA Product Code
OBR FDA UDI
GMDN Term
Mouthguard, reusable FDA UDI

Classification

Device Class
U FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Mouthguard, reusable

GrindRelief PRO by Grind Guard Technologies, L.L.C. — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Mouthguard, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI de9793e2-95f3-4086-aa35-a6f8c86d44ba 36 fields · synced May 30, 2026