Manufacturer registered with FDA
Zentro Enterprise Pvt. Ltd.
RAJKOT, India. Lists 6 dental device types with FDA across 1 registered establishment.
- Device types listed
- 6
- Brands and models
- 6
- 510(k) clearances
- 0as applicant
- Markets registered in
- 1United States
- Establishments
- 1India
Devices listed with FDA
What Zentro Enterprise Pvt. Ltd. currently lists, by FDA device type, with the brand and model names on the listing.
| Device type | Category | Role | Brands and models | Listed since |
|---|---|---|---|---|
| All Precision AttachmentEGG · Class 1 | — | Maker | ATTACHMENT, PRECISION, ALL | 2019 |
| Abrasive DiskEHJ · Class 1 | Polishing & prophylaxis | Maker | DISK, ABRASIVE | 2019 |
| Dental Wax CarverEIK · Class 1 | Dental hand instruments | Maker | CARVER, WAX, DENTAL | 2019 |
| Dental Instrument HandleEJB · Class 1 | Dental hand instruments | Maker | HANDLE, INSTRUMENT, DENTAL | 2019 |
| Dental BurEJL · Class 1 | Dental burs & diamonds | Maker | BUR, DENTAL | 2019 |
| ArticulatorsEJP · Class 1 | Articulators & facebows | Maker | ARTICULATORS | 2019 |
Source: FDA establishment registration & device listing, 510(k) and product classification files · FDA data as of 2 Nov 2026 · snapshot 12 Nov 2026
Registered establishments
| Establishment | Location | What it does |
|---|---|---|
| ZENTRO ENTERPRISE PVT LTDFDA reg. 3015980617 | RAJKOT Gujarat, India | Manufacturer, Repacker / relabeler |
Sources
FDA establishment registration & device listing (search FDA, owner/operator 10061477). 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.