AKERVALL TECHNOLOGIES

FDA Device Registration & Listing · Saline, MI, US · Registration 3011547262

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
3011547262
FEI Number
3011547262
Entity Name
AKERVALL TECHNOLOGIES
City/State/Country
Saline, MI, US
Establishment Address
1512 Woodland Dr, Saline, MI 48176, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device
Owner / Operator
Akervall Technologies Inc. (Owner Number: 10048970)
Owner / Operator Contact Address
1512 Woodland Dr., Saline, MI 48176, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

SOVA Night Guard SOVA MAX SOVA Junior SOVA Aero Intuguard

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
ILH Splint, Hand, And Components Physical Medicine Class 1 890.3475 2024-02-06
OBR Mouthguard, Over-The-Counter Unknown Class U N/A 2015-03-26
EFT Cleanser, Denture, Over The Counter Dental Class 1 872.3520 2024-02-06
EHY Tray, Impression, Preformed Dental Class 1 872.6880 2024-02-06
BRW Protector, Dental Anesthesiology Class 1 868.5820 2023-02-07

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

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

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K902838 Denture Dynamic'S, Inc. DENTURE DYNAMIC'S DENTURE MAGIC 1990-09-06

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3041725026 Fill Mill Lakewood, NJ, US
3012316249 COMPASS HEALTH BRANDS (CORPORATE OFFICE) Middleburg Heights, OH, US
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3011547262. Last updated year: 2026. Please use registration number 3011547262 when referencing this establishment in official correspondence.
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