APEX DENTAL SLEEP LAB

FDA Device Registration & Listing · La Mesa, CA, US · Registration 3012716038

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
3012716038
FEI Number
3012716038
Entity Name
APEX DENTAL SLEEP LAB
City/State/Country
La Mesa, CA, US
Establishment Address
7863 La Mesa, Suite 204, La Mesa, CA 91942, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Apex Dental Sleep Lab (Owner Number: 10055016)
Owner / Operator Contact Address
7863 La Mesa Boulevard, #204, La Mesa, CA 91942, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

EMA Kava TAP EMA 3D Oasys Oral/Nasal Airway System MMRNA

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
LRK Device, Anti-Snoring Dental Class 2 872.5570 2017-05-24
LRK Device, Anti-Snoring Dental Class 2 872.5570 2019-12-16
LQZ Device, Jaw Repositioning Dental Class 2 872.5570 2019-12-16
LRK Device, Anti-Snoring Dental Class 2 872.5570 2017-05-24
LRK Device, Anti-Snoring Dental Class 2 872.5570 2024-07-03
LQZ Device, Jaw Repositioning Dental Class 2 872.5570 2024-07-03
LRK Device, Anti-Snoring Dental Class 2 872.5570 2017-05-24
LWF Dilator, Nasal Ear, Nose, Throat Class 1 874.3900 2017-05-24
LQZ Device, Jaw Repositioning Dental Class 2 872.5570 2021-12-29
LRK Device, Anti-Snoring Dental Class 2 872.5570 2021-12-29

Official Correspondent

Philip Bocala

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Apex Dental Sleep Lab
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
K122391 Medtronic Xomed, Inc. MEDTRONIC XOMED, INC. 2013-01-10

Similar Registrations

Registration Number Establishment Name Location
3030914478 GELB PRACTICE Dix Hills, NY, US
3017092365 APNOMED, INC. Bellevue, WA, US
3039643908 EMA-SLEEP INC Bastrop, TX, US
3007108578 TRUE FUNCTION LABORATORY INC La Mesa, CA, US
3006786034 Innovative Health Technologies (NZ) Limited Dunedin Otago, NZ
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3012716038. Last updated year: 2026. Please use registration number 3012716038 when referencing this establishment in official correspondence.
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