Exceed Unlimited

Exceed Unlimited is a prescription microneedling device for adults aged 22 and older. It mechanically punctures the skin with fine needles for treating specified facial wrinkles in…

Registry build 21.09.26

Exceed Unlimited is a prescription microneedling device for adults aged 22 and older. It mechanically punctures the skin with fine needles for treating specified facial wrinkles in Fitzpatrick skin types I to III and improving facial acne scar appearance in skin types I to IV.

A motor in the handpiece moves the needles in a replaceable cartridge. The user adjusts the operating frequency between 100 and 150 Hz and sets needle protrusion with a dial. The standard cartridge has six stainless steel microneedles and an internal safety membrane.

Listed Item

The Exceed Unlimited device is intended to create many, very tiny, microscopic punctures in the epidermal and dermal layers of the skin using sterile stainless steel needles. The Exceed Unlimited device consists of 7 component parts; Handpiece, sterile single use Safety needle cartridge, Handpiece holder, Barrier Sleeve, Battery, Charger incl. USB cable, power supply. The handpiece contains a motor that moves the needles. The handpiece receives power via a Li-Ion battery with an output of 3,7 V. The battery charger receives power from a standard 100-240V, 50- 60Hz, 0.45A wall socket transformer with an USB output of 5 V, 3.2A.

Power and Cartridge

The handpiece operates from a rechargeable lithium ion battery. Its sterile cartridge is for one patient use and cannot be reused. The wrinkle indication covers glabellar frown lines, periorbital lines and cheek folds.

10manufacturers in China registered for this device type
1catalogue number
3510(k) clearances naming this product code

Who Else Makes It

Concentrated in Beijing (4), Guangdong (4), Hebei (2). One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code QAI
Manufacturer City Province Registered as Device types
PAN-International Precision Electronic Co., Ltd. Dongguan Guangdong Contract manufacturer 4
Beijing Spiritlaser Science & Technology Co., Ltd. Beijing Beijing Contract manufacturer 21
Beijing Winkonlaser Technology Limited Beijing Beijing Contract manufacturer 14
Dongguan King Medical Technology Co., Ltd. Dongguan Guangdong Contract manufacturer 14
Beijing Beautemax Technology Limited Beijing Beijing Contract manufacturer 13
Beijing Perfectlaser Technology Co., Ltd. Beijing Beijing Manufacturer 12
Hebei Lufen Tech Co., Limited Xingtai Hebei Contract manufacturer 12
Sanhe Jumei Technology Co., Ltd. Sanhe Hebei Manufacturer 12
Guangzhou Ekai Electronic Technology Co., Ltd. Guangzhou Guangdong Contract manufacturer 1
Guangdong Carain Beauty Equipment Co., Ltd. Foshan Guangdong Contract manufacturer 1

Record

Regulatory record for Exceed Unlimited
Listed by Mt.derm GmbH, Germany
FDA product code QAI
Device type Powered Microneedle Device
Device class Class 2
Regulation 21 CFR 878.4430
Establishment Specification developer, Complaint-file establishment, Manufacturer
510(k) K233709
Record published 2026-05-22

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Prescription Prescription only
Label carries manufacturing date, serial number
Storage Storage environment temperature -4 to 113 °F; Storage environment humidity 20 to 80 % RH; Storage environment atmospheric pressure 54 to 107 KiloPascal; Handling environment temperature 59 to 77 °F; Handling environment humidity 30 to 75 % RH; Handling environment atmospheric pressure 54 to 107 KiloPascal

Catalogue Numbers

Catalogue numbers for Exceed Unlimited
Catalogue number Size Status
CG100206USMP In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
ellacor Cytrellis Biosystems, Inc. 25
Collagen P.I.N. Induction Therapies, LLC 9
Footswitch Mt.derm GmbH 5
SkinPen Precision Elite Bellus Medical, LLC 4
Exceed Mt.derm GmbH 4
Safety Needle Cartridge 6-MNP 1.5 Exceed US Mt.derm GmbH 3
SkinPen Precision Treatment Kits Bellus Medical, LLC 3
CytoPen S2 Emage Medical, LLC 3
Dp4 Equipmed USA B.V. 3
PRO Pen Microneedling System Dermalogica, LLC 1
Xcellarispro Twist Control unit Dermaroller GmbH 1
Eclipse EVO Microneedling Cartridge Eclipse, Inc. 1

Showing 12 of 43. All products under Powered Microneedle Device

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K233709 2024-02-23
K182407 2019-07-19
K180778 2018-09-07

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer