Is this your brand? Sign in to claim ownership.

Sign in to claim this brand

POMEE CORPORATION

US

Last updated May 23, 2026

What POMEE CORPORATION makes

Pomee Corporation manufactures reusable dental instruments, including orthodontic pliers, manual dental scalers, tooth extraction forceps, surgical scissors, rubber dam clamps, periosteal elevators, suturing needle holders, and dental spatulas. These tools are designed for use in dental procedures such as extractions, scaling, suturing, and orthodontic adjustments. The instruments are intended for single-patient or multi-patient reuse under proper sterilization protocols. Their product line covers both general dental and surgical applications within oral healthcare settings.

The company’s devices are classified under Class I in the FDA’s regulatory framework and are listed in the FDA’s Unique Device Identifier (UDI) database. These instruments are intended for commercial distribution within the United States, adhering to applicable FDA requirements for medical devices. No additional regulatory bodies or international listings are referenced in the available data.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does Pomee Corporation manufacture?

Pomee Corporation specializes in reusable dental instruments, including orthodontic pliers for adjusting braces, manual dental scalers for removing plaque, tooth extraction forceps for removing teeth, dental surgical scissors for cutting tissue, rubber dam clamps for isolating teeth during procedures, periosteal elevators for lifting gum tissue, suturing needle holders for stitching, and dental spatulas for mixing materials. These tools are designed for use in general dental and surgical applications within oral healthcare settings.

Where is Pomee Corporation based, and where are its devices primarily distributed?

Pomee Corporation is based in the United States. Its devices are intended for commercial distribution within the U.S., where they must comply with applicable FDA requirements for medical devices. The company’s focus is on the domestic market, and no international regulatory listings or distribution details are referenced in the available data.

Which regulatory registries or databases list Pomee Corporation’s devices?

Pomee Corporation’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. The UDI system helps track and identify medical devices in the U.S. regulatory framework. Since these devices fall under Class I classification, they are subject to general controls but do not require additional pre-market approval or listing in other major international registries based on the available information.

How are Pomee Corporation’s devices classified under FDA regulations?

Pomee Corporation’s devices are classified under Class I in the FDA’s regulatory framework. Class I devices are generally considered to pose the lowest risk and are subject to general controls, such as registration, listing, and good manufacturing practices (GMP). This classification applies to reusable dental instruments like pliers, scalers, and forceps, which are intended for routine use in dental procedures without carrying significant risk to patients.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
US
Address
—
Website
—
LinkedIn
—
Facebook
—
Email
—
Phone
—
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
645717646

Catalogue (763)

Page 2 of 16
DeviceModel / ReferenceRegistriesClassStatus
Pomee 716-523
FDA UDI
Class IActive
Pomee 704-940
FDA UDI
Class IActive
Pomee 7210
FDA UDI
Class IActive
Pomee 725-7650
FDA UDI
Class IActive
Pomee 707-876
FDA UDI
Class IActive
Pomee 713-250
FDA UDI
Class IActive
Pomee 711-630
FDA UDI
Class IActive
Pomee 7134-W
FDA UDI
Class IActive
Pomee 711-710
FDA UDI
Class IActive
Pomee 755-0008
FDA UDI
Class IActive
Pomee 712-420
FDA UDI
Class IActive
Pomee 713-275
FDA UDI
Class IActive
Pomee 705-890
FDA UDI
Class IActive
Pomee 7121
FDA UDI
Class IActive
Pomee 735-5020
FDA UDI
Class IActive
Pomee 705-240
FDA UDI
Class IActive
Pomee 723-4250
FDA UDI
Class IActive
Pomee 724-1135
FDA UDI
Class IActive
Pomee 705-740
FDA UDI
Class IActive
Pomee 705-900
FDA UDI
Class IActive
Pomee 711-708
FDA UDI
Class IActive
Pomee 735-0050
FDA UDI
Class IActive
Pomee 704-520
FDA UDI
Class IActive
Pomee 702-120
FDA UDI
Class IActive
Pomee 701-010
FDA UDI
Class IActive
Pomee 704-945
FDA UDI
Class IActive
Pomee 702-450
FDA UDI
Class IActive
Pomee 713-304
FDA UDI
Class IActive
Pomee 702-602
FDA UDI
Class IActive
Pomee 704-385
FDA UDI
Class IActive
Pomee 712-111
FDA UDI
Class IActive
Pomee 707-835
FDA UDI
Class IActive
Pomee 711-045
FDA UDI
Class IActive
Pomee 704-786AR
FDA UDI
Class IActive
Pomee 706-159
FDA UDI
Class IActive
Pomee 711-610
FDA UDI
Class IActive
Pomee 713-125
FDA UDI
Class IActive
Pomee 702-288
FDA UDI
Class IActive
Pomee 701-215
FDA UDI
Class IActive
Pomee 702-295
FDA UDI
Class IActive
Pomee 7110
FDA UDI
Class IActive
Pomee 704-331
FDA UDI
Class IActive
Pomee 701-246
FDA UDI
Class IActive
Pomee 704-402
FDA UDI
Class IActive
Pomee 705-034
FDA UDI
Class IActive
Pomee 711-742OC
FDA UDI
Class IActive
Pomee 702-287
FDA UDI
Class IActive
Pomee 7122
FDA UDI
Class IActive
Pomee 707-810
FDA UDI
Class IActive
Pomee 7130
FDA UDI
Class IActive

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.

FDA Establishments (1)

Establishments registered with the FDA under this company group, matched by name.

  • Pomee Corporation Sialkot Punjab · PK FEI 3007064566