Contract manufacturerAPEX DENTAL SLEEP LAB (La Mesa, CA)CaliforniaDentalEar, nose and throatClass IIClass I
APEX DENTAL SLEEP LAB
Contract manufacturer ยท La Mesa, CA
FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified
- FDA registration
- 3012716038 (openFDA record; or search FDA's registration database)
- FEI number
- 3012716038
- Registered for
- FDA registration year 2026
- Establishment types
- Manufacturer; Contract manufacturer; Repackager or relabeler
- Owner or operator
- Apex Dental Sleep Lab (FDA owner/operator no. 10055016)
- Registered address
- 7863 La Mesa, Suite 204, La Mesa, CA 91942
- Contract listings
- 4 device listings, 3 product codes, first listed May 24, 2017
- Certification
- Not verified. We have no certification data for this facility yet.
Devices listed as contract work
Each row is an FDA product code this facility lists under its contract establishment type, with the date of its earliest such listing.
| Product code | Device (FDA name) | Class | Category | Role | First listed |
|---|
| LQZ | Device, Jaw Repositioning | Class II | Dental | Contract manufacturing | Dec 29, 2021 |
| LRK | Device, Anti-Snoring | Class II | Dental | Contract manufacturing | May 24, 2017 |
| LWF | Dilator, Nasal | Class I | Ear, nose and throat | Contract manufacturing | May 24, 2017 |