Manufacturer registered with FDA
Apothecaries Sundries Mfg Pvt Ltd
Gurugram, India. Lists 1 dental device type with FDA across 1 registered establishment.
- Device types listed
- 1
- Brands and models
- 2
- 510(k) clearances
- 0as applicant
- Markets registered in
- 5133 registrations outside the US
- Establishments
- 1India
Registered in 5 markets
Where regulators' registries name Apothecaries Sundries Mfg Pvt Ltd 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 | Apothecaries Sundries Mfg Pvt Ltd | 1 device types | — | Below |
| India | CDSCO | Registration holder | Apothecaries Sundries Mfg. Private LimitedApothecaries Sundries Mfg. Co. | 120 | 2021–2025 | Pure Global AI |
| Colombia | INVIMA | Manufacturer | APOTHECARIES SUNDRIES MFG CO | 6 | — | Pure Global AI |
| Tanzania | TMDA | Manufacturer | Apothecaries Sundries Mfg. Pvt. LtdAPOTHECARIES SUNDRIES MFG. CO. | 5 | 2024–2025 | Pure Global AI |
| Peru | DIGEMID | Manufacturer | APOTHECARIES SUNDRIES MFG. PRIVATE LIMITED | 2 | 2018–2019 | 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 Apothecaries Sundries Mfg 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 |
|---|---|---|---|---|
| Suction Operatory UnitEBR · Class 1 | Suction & evacuation units | Maker | ASCOComfosmart | 2009 |
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 |
|---|---|---|
| APOTHECARIES SUNDRIES MFG PVT LTDFDA reg. 3007123908 | GURUGRAM Haryana, India | Manufacturer |
Sources
FDA establishment registration & device listing (search FDA, owner/operator 10026475). 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.