Emerald Instruments
Country not established FDA
Part of Emerald Instruments
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA establishment
What Emerald Instruments makes
Emerald Instruments manufactures dental instruments focused on tooth extraction, including specialized forceps designed for precise removal procedures. Their product line centers on tools intended for oral surgery and general dentistry applications, ensuring ergonomic and functional design for clinical use.
The company’s portfolio is classified under FDA’s Class I medical devices, indicating low-to-moderate risk and subject to general controls. Their products are listed in the FDA’s Unique Device Identifier (UDI) database, adhering to U.S. regulatory requirements for tracking and identification. The manufacturer operates from the United States.
Catalogue
- GUDID
Company details
- DUNS number
- 645518940
FDA establishments
- Emerald Instruments SIALKOT Punjab · PK FEI 3005973280
Frequently asked questions
How many devices does EMERALD INSTRUMENTS have in the registry?
The registry currently lists 1 device for EMERALD INSTRUMENTS. Devices recorded under merged duplicate company entries are counted once.
Which registries list EMERALD INSTRUMENTS's devices?
Among its 1 most recently registered device, EMERALD INSTRUMENTS has devices listed in FDA GUDID (1 device).
What risk classes do EMERALD INSTRUMENTS's devices fall under?
Among its 1 most recently registered device, the classes recorded for EMERALD INSTRUMENTS's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from EMERALD INSTRUMENTS in the registry?
The most recently registered devices listed for EMERALD INSTRUMENTS include Extracting Forceps Fig. 1.
Which FDA establishments are linked to EMERALD INSTRUMENTS?
1 FDA establishment is linked to EMERALD INSTRUMENTS in the registry; they are listed on the company page.