Extraction Forceps, English Pattern, #17 for Upper Right Molars Xcision-Line® | Helmut Zepf No. 12.017.00Z
English pattern extraction forceps upper right molars are precision-engineered dental instruments designed to facilitate safe, controlled tooth removal in the upper right molar region. Manufactured by Helmut Zepf GmbH in Germany, this instrument carries the designation #17 and belongs to the Xcision-Line® product series, reflecting a commitment to consistent clinical performance and instrument longevity.
Product Overview
The #17 English pattern extraction forceps upper right molars instrument features the classic English pattern design, which offers a well-established grip geometry suited to the anatomy of upper right molar extractions. The Xcision-Line® designation indicates that this forceps belongs to Helmut Zepf's specialized instrument line, developed for demanding clinical environments where reliability and precision are essential.
Key Features
- English pattern design optimized for upper right molar anatomy
- Part of the Xcision-Line® series by Helmut Zepf GmbH
- Manufactured in Germany to high quality standards
- Instrument reference: Helmut Zepf No. 12.017.00Z
- Designed for ergonomic handling and controlled extraction force
Made in Germany

Helmut Zepf GmbH has a long-standing reputation for manufacturing dental instruments in Germany. Each instrument in the Xcision-Line® range reflects this heritage of precision craftsmanship, making it a reliable choice for dental professionals who demand consistent results.
FAQ
What procedure is this forceps designed for? This instrument is specifically designed for the extraction of upper right molars using the English pattern technique, providing the clinician with controlled grip and appropriate angulation.
What is the Xcision-Line®? The Xcision-Line® is a dedicated product series from Helmut Zepf GmbH, developed to meet professional dental standards with a focus on precision and durability.
Is this instrument suitable for reprocessing? As a dental extraction instrument, it is generally intended for reprocessing in accordance with applicable clinical guidelines; please consult the manufacturer's documentation for specific reprocessing instructions.
