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Sign in to claim this brandENDOPERFECTION LIMITED
US
Last updated May 23, 2026
What ENDOPERFECTION LIMITED makes
Endoperfection Limited manufactures single-use rotary and reciprocating endodontic files, such as the VaryFlex Neo series, designed for root canal shaping and cleaning. Their reusable products include endodontic enlargers, serrated broaches, and obturation material distribution endpieces like the Lentulo and Peezo Reamers, which assist in canal preparation and filling procedures.
These devices are classified as Class I under FDA regulations and are listed in the FDA’s Unique Device Identifier (UDI) database. The company 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 Endoperfection Limited manufacture?
Endoperfection Limited specializes in endodontic devices used primarily in root canal treatment. Their product line includes single-use rotary and reciprocating files (like the VaryFlex Neo series) for shaping and cleaning root canals, as well as reusable tools such as endodontic enlargers, serrated broaches, and obturation material distribution endpieces (e.g., Lentulo and Peezo Reamers). These tools are designed to assist dentists in preparing and filling root canals efficiently.
Where is Endoperfection Limited based?
Endoperfection Limited is headquartered in the United States. The company’s location ensures compliance with U.S. regulatory standards, including those governing medical devices used in dental procedures.
Which regulatory registries or databases list Endoperfection Limited’s devices?
Endoperfection Limited’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry helps track and identify medical devices authorized for use in the U.S., ensuring transparency and traceability for healthcare providers and regulators.
How are Endoperfection Limited’s devices classified under FDA regulations?
Endoperfection Limited’s devices are classified as Class I under FDA regulations. This classification applies to low-risk devices that pose minimal potential harm to patients, such as many endodontic files and reusable tools used in controlled dental procedures. Class I devices typically undergo general controls rather than specialized premarket reviews.
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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- 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
- 224419290
Catalogue (161)
Page 4 of 4| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| VaryFlex Taper, VFTF3, 31mm | VFTF331 | FDA UDI | Class I | Active |
| VaryFlex Reciprocating, VFRF 50, 21mm | VFRF2150 | FDA UDI | Class I | Active |
| VaryFlex Flow, VFF 25mm Size 45/04 | VFF254504 | FDA UDI | Class I | Active |
| Lentulo, 30, 25 | EPC2530 | FDA UDI | Class I | Active |
| Lentulo, 40, 29 | EPC2940 | FDA UDI | Class I | Active |
| Lentulo, 25, 21 | EPC2125 | FDA UDI | Class I | Active |
| VaryFlex Flow, VFF 21mm Size 45/04 | VFF214504 | FDA UDI | Class I | Active |
| Gates Gliddens, 2, 32 | ESG322 | FDA UDI | Class I | Active |
| VaryFlex Taper, VFTF4, 25mm | VFTF425 | FDA UDI | Class I | Active |
| Peezo Reamers, 6, 28 | ESP286 | FDA UDI | Class I | Active |
| VaryFlex Neo Treatment Pack, VFNeo15/04 x 3, VFNeo 25/04 x 3, 25mm | VFNEOTP25 | FDA UDI | Class I | Active |
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FDA Establishments (1)
Establishments registered with the FDA under this company group, matched by name.
- Endoperfection Ltd Worcester Worcestershire · GB FEI 3019567808