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Respire Medical Holding

US

Last updated May 23, 2026

What Respire Medical Holding makes

Respire Medical Holding manufactures orthodontic appliances, including the Respire Pink Series with DentiTrac, Respire Pink Series-Herbst-EF, and Respire Blue Series-EF. These devices are designed for orthodontic treatment, such as space management and jaw alignment, using removable or semi-permanent appliances.

The company’s products fall under FDA Class II devices and are listed via 510(k) clearance. The manufacturer is based in the United States.

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 Respire Medical Holding manufacture?

Respire Medical Holding specializes in orthodontic appliances. Their devices include the Respire Pink Series with DentiTrac, Respire Pink Series-Herbst-EF, and Respire Blue Series-EF. These products are designed for orthodontic treatment, such as managing dental spacing and aligning the jaw using removable or semi-permanent appliances.

Where is Respire Medical Holding based?

Respire Medical Holding is headquartered in the United States. The company’s location is relevant for understanding its regulatory framework and compliance with U.S. medical device standards.

Which regulatory registries or databases list Respire Medical Holding’s devices?

Respire Medical Holding’s devices are listed in the FDA’s 510(k) clearance registry. This clearance process is required for Class II devices in the U.S., ensuring they meet regulatory requirements before commercial distribution.

How are Respire Medical Holding’s devices classified under U.S. regulations?

Respire Medical Holding’s devices fall under FDA Class II classification. This classification applies to devices that pose moderate risk and require special controls beyond general controls to ensure safety and effectiveness, such as orthodontic appliances.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
US
Address
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Catalogue (32)

DeviceModel / ReferenceRegistriesClassStatus
Blue Series - EF SB030US
FDA UDI
Class IIActive
Blue Series - H/S SB020US
FDA UDI
Class IIActive
Pink Series - H/S SP020US
FDA UDI
Class IIActive
Respire Pink EF+ SPP030US
FDA UDI
Class IIUnknown
Pink Series - EF SP030US
FDA UDI
Class IIActive
Respire Pink+ H/S SPP020US
FDA UDI
Class IIUnknown
Respire Pink+ Hard SPP000US
FDA UDI
Class IIUnknown
Respire Pink AT EF SPAT030US
FDA UDI
Class IIActive
Respire Pink Series Micro with DentiTrac SPMD000US
FDA UDI
Class IIActive
Pink Series - Hard SP000US
FDA UDI
Class IIActive
Respire Pink AT Hard/Soft SPAT020US
FDA UDI
Class IIActive
Pink Micro - EF SPM030US
FDA UDI
Class IIActive
Respire Pink+ H/S with DentiTrac SPPD020US
FDA UDI
Class IIUnknown
Respire Pink+ Hard with DentiTrac SPPD000US
FDA UDI
Class IIUnknown
Pink Micro - Hard SPM001US
FDA UDI
Class IIActive
Respire Pink Series Micro H/S with DentiTrac PSMD020US
FDA UDI
Class IIActive
Respire Pink Series EF with DentiTrac SPD030US
FDA UDI
Class IIActive
Blue + Hard SBP000US
FDA UDI
Class IIActive
Respire Pink AT Hard SPAT000US
FDA UDI
Class IIActive
Blue + Hard/Soft SBP020US
FDA UDI
Class IIActive
Pink Micro - H/S SPM020US
FDA UDI
Class IIActive
Respire Pink Series with DentiTrac - H SPD000US
FDA UDI
Class IIActive
Blue EF + Hard/Soft SBP040US
FDA UDI
Class IIActive
Blue Series - Hard SB000US
FDA UDI
Class IIActive
Blue EF + Hard SBP030US
FDA UDI
Class IIActive
Respire Pink EF+ with DentiTrac SPPD030US
FDA UDI
Class IIUnknown
Respire Pink Series H/S with DentiTrac SPD020US
FDA UDI
Class IIActive
Respire Pink Series EF Micro with DentiTrac SPMD030US
FDA UDI
Class IIActive
Respire Pink Series with DentiTrac K170692
FDA 510(k)
Class IIActive
Respire Pink Series-Herbst-EF K150572
FDA 510(k)
Class IIActive
Respire Pink AT (Hard, Hard/Soft, EF) K192127
FDA 510(k)
Class IIActive
Respire Blue Series-EF K152292
FDA 510(k)
Class IIActive

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