Manufacturer registered with FDA
Steiner Biotechnology LLC
Henderson, NV, United States. Lists 2 dental device types with FDA across 1 registered establishment.
- Device types listed
- 2
- Brands and models
- 4
- 510(k) clearances
- 0as applicant
- Markets registered in
- 1United States
- Establishments
- 1United States
Devices listed with FDA
What Steiner Biotechnology LLC currently lists, by FDA device type, with the brand and model names on the listing.
| Device type | Category | Role | Brands and models | Listed since |
|---|---|---|---|---|
| Synthetic Bone Grafting MaterialLYC · Class 2 | Bone grafts & membranes | Maker | OsseoConductSinus GraftSocket Graft | 2007 |
| Dental CementEMA · Class 2 | Dental cements | Maker | Oral Bond | 2017 |
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
Steiner Biotechnology LLC 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: Steiner Laboratories (4), Steiner Laboratories Div of Steiner Healthcare, LLC (1).
| Decided | 510(k) | Device | Applicant | Device type |
|---|---|---|---|---|
| 6 Jun 2016 | K142130 | ORAL BOND | Steiner Laboratories | EMA Dental Cement |
| 27 Jan 2012 | K113049 | SOCKET GRAFT | Steiner Laboratories | LYC Synthetic Bone Grafting Material |
| 26 Oct 2010 | K101718 | OSSEOCONDUCT | Steiner Laboratories Div of Steiner Healthcare, LLC | LYC Synthetic Bone Grafting Material |
| 28 Nov 2006 | K063010 | REGEN BIOCEMENT | Steiner Laboratories | LYC Synthetic Bone Grafting Material |
| 9 Jun 2006 | K052493 | SOCKET GRAFT | Steiner Laboratories | LYC Synthetic Bone Grafting Material |
Registered establishments
| Establishment | Location | What it does |
|---|---|---|
| STEINER BIOTECHNOLOGYFDA reg. 3005138409 | Henderson, NV, United States | Manufacturer |
Sources
FDA establishment registration & device listing (search FDA, owner/operator 9072756). 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.