Manufacturer registered with FDA
Groman, Inc.
Pompano Beach, FL, United States. Lists 1 dental device type with FDA across 1 registered establishment, and holds 1 510(k) clearance as applicant.
- Device types listed
- 1
- Brands and models
- 4
- 510(k) clearances
- 12003–2003
- Markets registered in
- 1United States
- Establishments
- 1United States
510(k) clearances per year, 2000–2026
Devices listed with FDA
What Groman, 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 |
|---|---|---|---|---|
| AirbrushKOJ · Class 2 | — | Maker | EtchMasterPowderMasterPrepMasterProphyMaster | 2007 |
Source: FDA establishment registration & device listing, 510(k) and product classification files · FDA data as of 2 Nov 2026 · snapshot 12 Nov 2026
510(k) clearances
Clearances on which FDA names Groman, Inc. as the applicant.
Some of these clearances are listed with FDA today by another company: Reliance Orthodontic Products, Inc. (1).
Registered establishments
| Establishment | Location | What it does |
|---|---|---|
| GROMAN INC.FDA reg. 3004361444 | Coconut Creek, FL, United States | Contract manufacturer, Manufacturer, Repacker / relabeler, Specification developer |
Sources
FDA establishment registration & device listing (search FDA, owner/operator 9054890). 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.