Registered with FDA
Olson Dental Laboratory, Inc.
Clinton Township, MI, United States. Lists 6 dental device types with FDA across 1 registered establishment.
- Device types listed
- 6
- Brands and models
- 7
- 510(k) clearances
- 0as applicant
- Markets registered in
- 1United States
- Establishments
- 1United States
Devices listed with FDA
What Olson Dental Laboratory, Inc. currently lists, by FDA device type, with the brand and model names on the listing.
| Device type | Category | Role | Brands and models | Listed since |
|---|---|---|---|---|
| Rebasing Repairing Relining Denture ResinEBI · Class 2 | Denture resins & teeth | Lister | acrylicresin | 2013 |
| Preformed ClaspEHP · Class 1 | — | Lister | Duracetal | 2013 |
| Porcelain PowderEIH · Class 2 | Dental ceramics & zirconia | Lister | Powder, Porcelain | 2013 |
| Base Metal AlloyEJH · Class 2 | Dental alloys | Lister | Alloy, Base Metal | 2013 |
| Gold-Based Noble Metal AlloyEJT · Class 2 | Dental alloys | Lister | Alloy, Gold based noble metal | 2013 |
| Teeth Plastic DentureELM · Class 2 | Denture resins & teeth | Lister | Teeth | 2013 |
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
Olson Dental Laboratory, Inc. 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: Metoxit AG (1), Valplast Intl. Corp. (1), GC America Inc. (1), Inovativ, LLC (1), Dentsply Intl., Inc. (1).
| Decided | 510(k) | Device | Applicant | Device type |
|---|---|---|---|---|
| 31 Oct 2007 | K072569 | METOXIT CAM-BLANKS | Metoxit AG | EIH Porcelain Powder |
| 7 Apr 2006 | K060507 | VALPLAST YAMAHACHI TEETH | Valplast Intl. Corp. | ELM Teeth Plastic Denture |
| 7 Jul 2005 | K051358 | NATURE-CRYL HI PLUS | GC America Inc. | EBI Rebasing Repairing Relining Denture Resin |
| 29 Aug 2002 | K022032 | ACETAL | Inovativ, LLC | EHP Preformed Clasp |
| 6 Oct 1999 | K992956 | LUCITONE FRS FLEXIBEL DENTAL RESIN | Dentsply Intl., Inc. | EBI Rebasing Repairing Relining Denture Resin |
Registered establishments
| Establishment | Location | What it does |
|---|---|---|
| OLSON GLOBAL LABORATORYFDA reg. 3005344553 | CLINTON TOWNSHIP, MI, United States | Repacker / relabeler |
Other names on FDA records
Olson Global Laboratory
Sources
FDA establishment registration & device listing (search FDA, owner/operator 9077241). 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.