Registered with FDA
Press-Master, LLC DBA Aesthetic Press
New Port Richey, FL, United States. Lists 1 dental device type with FDA across 1 registered establishment.
- Device types listed
- 1
- Brands and models
- 3
- 510(k) clearances
- 0as applicant
- Markets registered in
- 1United States
- Establishments
- 1United States
Devices listed with FDA
What Press-Master, LLC DBA Aesthetic Press currently lists, by FDA device type, with the brand and model names on the listing.
| Device type | Category | Role | Brands and models | Listed since |
|---|---|---|---|---|
| Porcelain PowderEIH · Class 2 | Dental ceramics & zirconia | Lister | AP Volution MAP Volution SAPVolution S | 2007 |
Source: FDA establishment registration & device listing, 510(k) and product classification files · FDA data as of 2 Nov 2026 · snapshot 12 Nov 2026
Also lists devices cleared under other names
Press-Master, LLC DBA Aesthetic Press lists these devices with FDA today. The clearance names a different applicant, as happens after a rename, an acquisition or a private-label agreement.
Original applicants: Shenzhen Xiangtong Co., Ltd. (1), Aesthetic-Press, LLC (1), Midatlantic Division of Dentrex, Inc. (1).
| Decided | 510(k) | Device | Applicant | Device type |
|---|---|---|---|---|
| 8 Dec 2025 | K252789 | Glass Ceramic | Shenzhen Xiangtong Co., Ltd. | EIH Porcelain Powder |
| 5 Jun 2017 | K163228 | APVolution System | Aesthetic-Press, LLC | EIH Porcelain Powder |
| 25 May 2000 | K000680 | VISION ESTHETIC PORCELAIN SYSTEM | Midatlantic Division of Dentrex, Inc. | EIH Porcelain Powder |
Registered establishments
| Establishment | Location | What it does |
|---|---|---|
| Press-Master, LLC DBA Aesthetic PressFDA reg. 3006146796 | Palm Harbor, FL, United States | Repacker / relabeler |
Sources
FDA establishment registration & device listing (search FDA, owner/operator 9098079). FDA 510(k) premarket notification file. FDA data as of 2 Nov 2026; snapshot 12 Nov 2026. The location shown is the address on FDA's record.