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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 14 of 16
DeviceModel / ReferenceRegistriesClassStatus
Pomee 701-220
FDA UDI
Class IActive
Pomee 716-532
FDA UDI
Class IActive
Pomee 704-140
FDA UDI
Class IActive
Pomee 7523
FDA UDI
Class IActive
Pomee 7509
FDA UDI
Class IActive
Pomee 716-533
FDA UDI
Class IActive
Pomee 708-305
FDA UDI
Class IActive
Pomee 7132
FDA UDI
Class IActive
Pomee 7103
FDA UDI
Class IActive
Pomee 702-292
FDA UDI
Class IActive
Pomee 708-90
FDA UDI
Class IActive
Pomee 765-7550
FDA UDI
Class IActive
Pomee 712-110
FDA UDI
Class IActive
Pomee 707-885
FDA UDI
Class IActive
Pomee 704-965
FDA UDI
Class IActive
Pomee 704-925
FDA UDI
Class IActive
Pomee 723-3070
FDA UDI
Class IActive
Pomee 716-519
FDA UDI
Class IActive
Pomee 722-1585
FDA UDI
Class IActive
Pomee 716-500
FDA UDI
Class IActive
Pomee 707-871
FDA UDI
Class IActive
Pomee 724-1175
FDA UDI
Class IActive
Pomee 742-2710
FDA UDI
Class IActive
Pomee 735-0060
FDA UDI
Class IActive
Pomee 713-305
FDA UDI
Class IActive
Pomee 705-320
FDA UDI
Class IActive
Pomee 704-336
FDA UDI
Class IActive
Pomee 702-533
FDA UDI
Class IActive
Pomee 712-143
FDA UDI
Class IActive
Pomee 701-205
FDA UDI
Class IActive
Pomee 705-880
FDA UDI
Class IActive
Pomee 702-534
FDA UDI
Class IActive
Pomee 701-265
FDA UDI
Class IActive
Pomee 711-020
FDA UDI
Class IActive
Pomee 7119
FDA UDI
Class IActive
Pomee 713-301
FDA UDI
Class IActive
Pomee 712-255
FDA UDI
Class IActive
Pomee 708-300
FDA UDI
Class IActive
Pomee 719-4000
FDA UDI
Class IActive
Pomee 712-117
FDA UDI
Class IActive
Pomee 703-335
FDA UDI
Class IActive
Pomee 708-055G
FDA UDI
Class IActive
Pomee 703-190
FDA UDI
Class IActive
Pomee 7528
FDA UDI
Class IActive
Pomee 712-125
FDA UDI
Class IActive
Pomee 707-905
FDA UDI
Class IActive
Pomee 705-745
FDA UDI
Class IActive
Pomee 704-957
FDA UDI
Class IActive
Pomee 716-555
FDA UDI
Class IActive
Pomee 722-1500
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