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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 1 of 16
DeviceModel / ReferenceRegistriesClassStatus
Pomee 725-7656
FDA UDI
Class IActive
Pomee 716-550
FDA UDI
Class IActive
Pomee 7205
FDA UDI
Class IActive
Pomee 707-305
FDA UDI
Class IActive
Pomee 7111
FDA UDI
Class IActive
Pomee 706-151
FDA UDI
Class IActive
Pomee 707-400
FDA UDI
Class IActive
Pomee 7213-A
FDA UDI
Class IActive
Pomee 702-364
FDA UDI
Class IActive
Pomee 765-7656
FDA UDI
Class IActive
Pomee 713-124
FDA UDI
Class IActive
Pomee 712-145
FDA UDI
Class IActive
Pomee 713-110
FDA UDI
Class IActive
Pomee 765-6360
FDA UDI
Class IActive
Pomee 7217
FDA UDI
Class IActive
Pomee 716-524
FDA UDI
Class IActive
Pomee 704-981
FDA UDI
Class IActive
Pomee 7521
FDA UDI
Class IActive
Pomee 7251
FDA UDI
Class IActive
Pomee 7501
FDA UDI
Class IActive
Pomee 706-322
FDA UDI
Class IActive
Pomee 703-300
FDA UDI
Class IActive
Pomee 712-108
FDA UDI
Class IActive
Pomee 702-529
FDA UDI
Class IActive
Pomee PCAP
FDA UDI
Class IActive
Pomee 706-325U
FDA UDI
Class IActive
Pomee 705-730
FDA UDI
Class IActive
Pomee 711-694
FDA UDI
Class IActive
Pomee 704-955
FDA UDI
Class IActive
Pomee 712-134
FDA UDI
Class IActive
Pomee 711-067JOC
FDA UDI
Class IActive
Pomee 706-154
FDA UDI
Class IActive
Pomee 702-601
FDA UDI
Class IActive
Pomee 704-997
FDA UDI
Class IActive
Pomee 707-205
FDA UDI
Class IActive
Pomee 707-310
FDA UDI
Class IActive
Pomee 704-941
FDA UDI
Class IActive
Pomee 704-860
FDA UDI
Class IActive
Pomee 722-1155
FDA UDI
Class IActive
Pomee 712-102
FDA UDI
Class IActive
Pomee 701-210
FDA UDI
Class IActive
Pomee 707-940
FDA UDI
Class IActive
Pomee 7129
FDA UDI
Class IActive
Pomee 706-326
FDA UDI
Class IActive
Pomee PCRF
FDA UDI
Class IActive
Pomee 707-500
FDA UDI
Class IActive
Pomee 711-550
FDA UDI
Class IActive
Pomee 712-339
FDA UDI
Class IActive
Pomee 7120
FDA UDI
Class IActive
Pomee 709-255
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