















Dr. Pen A11: Pro-Grade Inductive Base Microneedling Workstation
✅ Inductive Base-Station eliminates table-contact cross-contamination. ✅ Pro-Grade Dermal Mapping motor ensures absolute depth precision. ✅ FDA-Registered facility manufactured & CE Certified for clinical safety.

Dr. Pen A11: Pro-Grade Inductive Base Microneedling Workstation
Product details
If you have any questions, you are always welcome to contact us. We'll get back to you as soon as possible, within 24 hours on weekdays.
-
Shipping Information
Use this text to answer questions in as much detail as possible for your customers.
-
Customer Support
Use this text to answer questions in as much detail as possible for your customers.
-
FAQ’s
Use this text to answer questions in as much detail as possible for your customers.
-
Contact Us
Use this text to answer questions in as much detail as possible for your customers.
Clinical Protocol: A11 Workstation Execution
Watch the official clinical demonstration of the Dr. Pen A11, highlighting the use of the inductive sterile base during mid-session pauses and proper dermal mapping techniques.

The Physics of Inductive Sterility
Placing a device on a non-sterile table mid-session is the leading cause of bacterial cross-contamination. The A11 eliminates this critical flaw with its smart Inductive Base . When paused, the device rests vertically, keeping open micro-needles completely isolated from surface pathogens.

FDA-Registered Clinical Safety
Severe skin remodeling requires strict safety protocols. The Dr. Pen A11 is manufactured in an FDA-Registered Facility, holds full CE Certification, and utilizes EO Sterilizedcartridges to provide the ultimate sterile environment for dermal mapping.
Clinical Protocol
Sterilization Verification
Unpack a single-use EO Sterilized cartridge.
Base Setup
Plug in the Inductive Base. Always return the A11 to the base when pausing. Never lay it flat on a table.
Depth Calibration
Use 0.25mm - 0.5mm for transdermal serum delivery. Use 1.0mm - 2.5mm strictly for structural scar remodeling.
Wound Healing
Erythema is required. Keep the skin sterile for 48 hours.
Technical Specifications
| Parameter | Specification |
|---|---|
E-E-A-T Certifications |
FDA-Registered Facility, CE, RoHS |
Sterilization Protocol |
EO (Ethylene Oxide) Gas Sterilization |
Workstation Architecture |
Smart Inductive Base + Wireless Device |
Motor Action |
Pro-Grade Dermal Mapping (Zero Torque-Loss) |
Depth Calibration |
0.0mm - 2.5mm |
✈️ Free Global Shipping
🛡️ 1-Year Warranty
FAQs
Please read our FAQs page to find out more.
Q1: Why is the Inductive Base critical for clinical safety?
A: Resting a device on a table mid-session invites pathogens into the cartridge. The A11’s base holds the device vertically, ensuring needles never touch unsterilized surfaces.
Q2: What is Dermal Mapping and how does the A11 achieve it?
A: Dermal mapping maintains exact needle penetration depth regardless of skin resistance. The A11’s pro-grade motor ensures that a 2.0mm setting delivers exactly 2.0mm of penetration without lateral drag.
Q3: Can the A11 treat deep, thick-tissue stretch marks?
A: Yes. Its sustained motor output and 2.5mm depth calibration induce the aggressive fibrosis required to remodel thick tissue.
Q4: Does the Inductive Base charge the device while resting?
A: Yes. The base acts as both a sterile resting station and an inductive charging dock, ensuring the pro-grade motor never loses torque.
Q5: Are the cartridges backwards compatible with older models?
A: No. The A11 utilizes a specific bayonet locking mechanism designed to handle the high torque of its pro-grade motor.
Q6: What is the expected downtime after a 1.5mm session?
A: Expect visible erythema (redness) resembling a sunburn for 24-48 hours. Petechiae (pinpoint bleeding) is the correct biological response for triggering Type I Collagen