A single GuideLock™ reference unit designed to stabilise edentulous surgical guides using a screw-retained, bone-anchored reference. Supplied complete with both standard and multi-unit caps for maximum intra-operative flexibility.
Patent Protected and Certified Worldwide - CE, UKCA and FDA
ALL IN STOCK - Global Delivery with DHL
Note for International customers: Importing this CE-marked Class I medical device. In Spain this may require a valid AEMPS operating licence for medical device importers to clear customs quickly. Pricing is without tax charges.
If you are in the UK 20% VAT is applied on check out. If you are ordering internationally, this will not be charged as you will be levied the appropriate charges as calculated by your country and their policies. These charges vary depending on country and import tax rates.
Product Description
GuideLock™ is a screw-retained reference system developed to improve the accuracy and stability of guided implant surgery in fully edentulous cases.
Unlike conventional mucosa-supported guides, GuideLock™ introduces a bone-anchored, two-part fixation reference, allowing the surgical guide to be rigidly stabilised and reproducibly seated between CBCT planning and clinical placement.
A recent peer-reviewed in vitro study - https://www.nature.com/articles/s41405-025-00361-5 - demonstrated that this fixation concept significantly reduced coronal and apical implant deviations when compared to conventional mucosa-supported guides, supporting its use in flapless edentulous workflows .
This single unit is ideal for:
• Replacement
• Case extension
• Evaluation prior to system adoption
What’s Included;
1) Scan Ladder GuideLock™ Reference Unit (Single)
2) Scan Ladder GuideLock™ Reference Units – 3 Pack
3) Scan Ladder GuideLock™ Complete Procedure Kit – 6 Reference Units
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6 × GuideLock™ reference screws
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6 × Standard caps
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6 × Multi-Unit (MUA) caps
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GuideLock™ drivers
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Lance bur
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Metal autoclave storage box
Key Clinical Benefits
• Bone-anchored reference improves guide stability
• Reduced reliance on mucosal support
• Compatible with digital guided surgery workflows
• Supplied with both cap options for flexibility
Intended Use
Scan Ladder GuideLock™ is a screw-retained reference system intended for transient intra-operative use during guided implant surgery and digital impression capture. It is designed to temporarily stabilise surgical guides and provide reproducible reference points for CBCT and intraoral scanning in edentulous workflows. The reference screw is inserted and removed within the same procedure and is not intended to remain in the body. GuideLock™ is supplied non-sterile; reference screws are single-use, and reusable accessories must be cleaned and sterilised prior to use in accordance with the Instructions for Use.
For professional dental use only.
See CE DOC and IFU
Manufacturer Name
Full Arch Technologies Limited
Manufaccturer’s Address
Unit 39, Hethel Engineering Centre, Hethel. NR148FB
Contact Information
Website: www.scanladder.com
Customer Support Email: info@scanladder.com
GMDN Code 64323
UDI-DI: 50700034025GUIDELOCKV6
EU EUDAMED UK-MF-000045401
EU Authorised Representative
Cert3global, Unipessoal Lda. Hermano Neves, n°
18, Piso 3, E7, 1600-477, Lisboa, Portugal
enquiry@cert3global.com
U.S. FDA Assigned Owner/Operator Number:
10091807
Registration Number: 3033436335
