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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
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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 3 of 16
DeviceModel / ReferenceRegistriesClassStatus
Pomee 712-109
FDA UDI
Class IActive
Pomee 703-470
FDA UDI
Class IActive
Pomee 724-1015
FDA UDI
Class IActive
Pomee 704-973
FDA UDI
Class IActive
Pomee 711-696
FDA UDI
Class IActive
Pomee 724-3010
FDA UDI
Class IActive
Pomee 704-820
FDA UDI
Class IActive
Pomee 702-285
FDA UDI
Class IActive
Pomee 707-220
FDA UDI
Class IActive
Pomee 7524
FDA UDI
Class IActive
Pomee 711-695
FDA UDI
Class IActive
Pomee 7215
FDA UDI
Class IActive
Pomee PCPH
FDA UDI
Class IActive
Pomee 7152
FDA UDI
Class IActive
Pomee 7154-C
FDA UDI
Class IActive
Pomee 711-690
FDA UDI
Class IActive
Pomee PCAT
FDA UDI
Class IActive
Pomee 711-030
FDA UDI
Class IActive
Pomee 712-440
FDA UDI
Class IActive
Pomee 712-142
FDA UDI
Class IActive
Pomee 7522
FDA UDI
Class IActive
Pomee 707-800
FDA UDI
Class IActive
Pomee 712-295
FDA UDI
Class IActive
Pomee 706-211
FDA UDI
Class IActive
Pomee 703-320
FDA UDI
Class IActive
Pomee 704-201
FDA UDI
Class IActive
Pomee 702-500
FDA UDI
Class IActive
Pomee 762-215
FDA UDI
Class IActive
Pomee 711-768
FDA UDI
Class IActive
Pomee 7139
FDA UDI
Class IActive
Pomee 712-141
FDA UDI
Class IActive
Pomee 702-502
FDA UDI
Class IActive
Pomee 704-850
FDA UDI
Class IActive
Pomee 722-1580
FDA UDI
Class IActive
Pomee 724-1052
FDA UDI
Class IActive
Pomee 704-100
FDA UDI
Class IActive
Pomee 707-870
FDA UDI
Class IActive
Pomee 7207
FDA UDI
Class IActive
Pomee 706-325L
FDA UDI
Class IActive
Pomee 702-521
FDA UDI
Class IActive
Pomee 712-040
FDA UDI
Class IActive
Pomee 702-210
FDA UDI
Class IActive
Pomee 711-525
FDA UDI
Class IActive
Pomee 702-375
FDA UDI
Class IActive
Pomee 711-620
FDA UDI
Class IActive
Pomee 765-6420
FDA UDI
Class IActive
Pomee 742-2730
FDA UDI
Class IActive
Pomee 711-533OC
FDA UDI
Class IActive
Pomee 704-810
FDA UDI
Class IActive
Pomee 711-533
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