GRINDGUARD INC

FDA Device Registration & Listing · San Francisco, CA, US · Registration 3017575849

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3017575849
FEI Number
3017575849
Entity Name
GRINDGUARD INC
City/State/Country
San Francisco, CA, US
Establishment Address
155 Jackson St, 1206, San Francisco, CA 94111, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
GrindGuard Inc (Owner Number: 10092861)
Owner / Operator Contact Address
155 Jackson St, 1206, San Francisco, CA 94111, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K251778
PMA Number
N/A

All Registered Proprietary Names

Remi Impression Material Remi Night Guard

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
EHY Tray, Impression, Preformed Dental Class 1 872.6880 2025-07-08
SHI Impression Material For Fabrication Of Patient-Matched Mouthguards, Over-The-Counter Dental Class 2 872.3660 2026-03-03
OCO Mouthguard, Migraine/Tension Headache Unknown Class U N/A 2026-03-03
OBR Mouthguard, Over-The-Counter Unknown Class U N/A 2026-03-03

Official Correspondent

Jennifer Day

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

GrindGuard Inc
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3017575849. Last updated year: 2026. Please use registration number 3017575849 when referencing this establishment in official correspondence.
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