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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 10 of 16
DeviceModel / ReferenceRegistriesClassStatus
Pomee 704-731
FDA UDI
Class IActive
Pomee 712-144
FDA UDI
Class IActive
Pomee 704-610
FDA UDI
Class IActive
Pomee 7529
FDA UDI
Class IActive
Pomee 704-918
FDA UDI
Class IActive
Pomee 7512
FDA UDI
Class IActive
Pomee 712-122
FDA UDI
Class IActive
Pomee 703-410
FDA UDI
Class IActive
Pomee 7128
FDA UDI
Class IActive
Pomee 707-805
FDA UDI
Class IActive
Pomee 711-204OC
FDA UDI
Class IActive
Pomee 705-060
FDA UDI
Class IActive
Pomee 706-327
FDA UDI
Class IActive
Pomee 7108
FDA UDI
Class IActive
Pomee 702-510G
FDA UDI
Class IActive
Pomee 712-136
FDA UDI
Class IActive
Pomee 705-105
FDA UDI
Class IActive
Pomee 704-401
FDA UDI
Class IActive
Pomee 708-055
FDA UDI
Class IActive
Pomee 703-195
FDA UDI
Class IActive
Pomee 711-701
FDA UDI
Class IActive
Pomee 704-733
FDA UDI
Class IActive
Pomee 705-130
FDA UDI
Class IActive
Pomee 708-255
FDA UDI
Class IActive
Pomee 711-765
FDA UDI
Class IActive
Pomee 702-522
FDA UDI
Class IActive
Pomee 708-010
FDA UDI
Class IActive
Pomee 706-217
FDA UDI
Class IActive
Pomee 725-7100
FDA UDI
Class IActive
Pomee 703-460
FDA UDI
Class IActive
Pomee 7125
FDA UDI
Class IActive
Pomee 707-300
FDA UDI
Class IActive
Pomee 711-140
FDA UDI
Class IActive
Pomee 711-204SDOC
FDA UDI
Class IActive
Pomee 707-855
FDA UDI
Class IActive
Pomee 705-620
FDA UDI
Class IActive
Pomee 711-751OC
FDA UDI
Class IActive
Pomee 765-7655
FDA UDI
Class IActive
Pomee 704-786AL
FDA UDI
Class IActive
Pomee 707-892
FDA UDI
Class IActive
Pomee 722-1110
FDA UDI
Class IActive
Pomee 7118
FDA UDI
Class IActive
Pomee 704-714
FDA UDI
Class IActive
Pomee 762-1510
FDA UDI
Class IActive
Pomee 712-132
FDA UDI
Class IActive
Pomee 707-898
FDA UDI
Class IActive
Pomee 724-1050
FDA UDI
Class IActive
Pomee 704-690
FDA UDI
Class IActive
Pomee 711-752
FDA UDI
Class IActive
Pomee 707-900
FDA UDI
Class IActive

Related Companies

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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