Manufacturer registered with FDA
Apollo Implant Components
Pabianice, Poland. Lists 1 dental device type with FDA across 1 registered establishment.
- Device types listed
- 1
- Brands and models
- 0
- 510(k) clearances
- 0as applicant
- Markets registered in
- 22 registrations outside the US
- Establishments
- 1Poland
Registered in 2 markets
Where regulators' registries name Apollo Implant Components as the manufacturer or the registration holder of a device.
| Market | Regulator | Named as | Name on the registry | Registrations | Issued | Records |
|---|---|---|---|---|---|---|
| United States | FDA | Manufacturer | Apollo Implant Components | 1 device types | — | Below |
| Israel | AMAR | Manufacturer | APOLLO IMPLANT COMPONENTS SP. Z O.O | 2 | — | Pure Global AI |
Outside the US the count is of all the company's device registrations in that market, dental or not · matched by company name and country · registry data read 12 Nov 2026
Devices listed with FDA
What Apollo Implant Components currently lists, by FDA device type, with the brand and model names on the listing.
| Device type | Category | Role | Brands and models | Listed since |
|---|---|---|---|---|
| Endosseous Dental Implant AccessoriesNDP · Class 1 | Implant instruments & surgical kits | Maker | — | 2025 |
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 |
|---|---|---|
| APOLLO IMPLANT COMPONENTS Sp. z o.o.FDA reg. 3032078590 | Pabianice Lodzkie, Poland | Manufacturer |
Other names on FDA records
Apollo Implant Components SP. Z O.O
Sources
FDA establishment registration & device listing (search FDA, owner/operator 10093014). 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.