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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
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LinkedIn
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Facebook
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Email
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Phone
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PRRC Contact
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EUDAMED SRN
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FDA FEI Number
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DUNS Number
645717646

Catalogue (763)

Page 5 of 16
DeviceModel / ReferenceRegistriesClassStatus
Pomee 7505
FDA UDI
Class IActive
Pomee 705-185
FDA UDI
Class IActive
Pomee 7101-A
FDA UDI
Class IActive
Pomee 7124
FDA UDI
Class IActive
Pomee 712-135
FDA UDI
Class IActive
Pomee 723-7073
FDA UDI
Class IActive
Pomee 716-522
FDA UDI
Class IActive
Pomee 704-772
FDA UDI
Class IActive
Pomee 765-6530
FDA UDI
Class IActive
Pomee 716-530
FDA UDI
Class IActive
Pomee PC-SS3
FDA UDI
Class IActive
Pomee 7138
FDA UDI
Class IActive
Pomee 712-101
FDA UDI
Class IActive
Pomee 711-595
FDA UDI
Class IActive
Pomee 7506
FDA UDI
Class IActive
Pomee 708-215
FDA UDI
Class IActive
Pomee 707-405
FDA UDI
Class IActive
Pomee 7109
FDA UDI
Class IActive
Pomee 704-765
FDA UDI
Class IActive
Pomee 7502
FDA UDI
Class IActive
Pomee 707-200
FDA UDI
Class IActive
Pomee 707-863
FDA UDI
Class IActive
Pomee 716-520
FDA UDI
Class IActive
Pomee 707-225
FDA UDI
Class IActive
Pomee 713-270
FDA UDI
Class IActive
Pomee 711-090
FDA UDI
Class IActive
Pomee 702-504
FDA UDI
Class IActive
Pomee 712-275
FDA UDI
Class IActive
Pomee 742-2720
FDA UDI
Class IActive
Pomee 7208
FDA UDI
Class IActive
Pomee 7127
FDA UDI
Class IActive
Pomee 712-121
FDA UDI
Class IActive
Pomee 702-320
FDA UDI
Class IActive
Pomee 702-365
FDA UDI
Class IActive
Pomee 704-730
FDA UDI
Class IActive
Pomee 724-3050
FDA UDI
Class IActive
Pomee 712-020
FDA UDI
Class IActive
Pomee 7151
FDA UDI
Class IActive
Pomee 7511
FDA UDI
Class IActive
Pomee 704-902
FDA UDI
Class IActive
Pomee 708-205
FDA UDI
Class IActive
Pomee 716-557
FDA UDI
Class IActive
Pomee 704-718
FDA UDI
Class IActive
Pomee 7219
FDA UDI
Class IActive
Pomee 713-126
FDA UDI
Class IActive
Pomee 762-195
FDA UDI
Class IActive
Pomee 725-6290
FDA UDI
Class IActive
Pomee 7154
FDA UDI
Class IActive
Pomee 701-245
FDA UDI
Class IActive
Pomee 724-4500
FDA UDI
Class IActive

Related Companies

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Authorities

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FDA Establishments (1)

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

  • Pomee Corporation Sialkot Punjab · PK FEI 3007064566