Skip to main content
Medical Recombinant Mussel Adhesive Protein Oral Ulcer Gel
Class II Medical Device Series

Medical Recombinant Mussel Adhesive Protein Oral Ulcer Gel

For relieving pain caused by wounds from oral ulcers, oral inflammation, dentures or surgery.

For relieving pain caused by wounds from oral ulcers, oral inflammation, dentures or surgery. This product is available in four models: Type I, Type II, Type III and Type IV. Type I consists of gel and soft tube (PE); Type II consists of gel and plastic bottle (PET); Type III consists of gel and aluminum-plastic tube (PE); Type IV consists of gel and disposable applicator tube (PP). The gel is composed of Recombinant Mussel Adhesive Protein, glycerin, trehalose, carbomer, triethanolamine, p-hydroxyacetophenone, 1,2-hexanediol, hydroxyethyl cellulose, ectoine and purified water. The product is supplied non-sterile.

MOQ

—

Sample Lead Time

7–14 days

Production Lead Time

25–35 days

Service Modes

OEM · ODM · Private Label

Specifications / Attributes

  • National Class II Medical Device Registration Certificate (Hunan Medical Device Registration)
  • Main Ingredients: Recombinant Mussel Adhesive Protein, glycerin, trehalose, carbomer, triethanolamine, p-hydroxyacetophenone, 1,2-hexanediol, hydroxyethyl cellulose, ectoine, purified water
  • Sterile (irradiation sterilization)
  • Supports custom OEM/ODM specifications and packaging

Technical Specifications

  • Registration No.: Xiang Medical Device Registration 20252170887
  • Model: Soft Tube (Type I), Plastic Bottle (Type II), Aluminum-Plastic Tube (Type III), Disposable Applicator Tube (Type IV)
  • Specification: 1–50 (multiple specifications available)
  • Packaging: Type I, Type II, Type III, Type IV
  • Sterility: Sterile

Why Weitai

Why Choose Weitai?

Dual cosmetics & medical device expertise — full-chain control from formula to mass production.

Weitai
Typical OEM Factory
Certification System
Dual cosmetics + Class II/III medical device qualifications (ISO 13485 / ISO 22716 / GMPC)
Cosmetics-only certification
Cleanroom Facility
Class 100,000 / 10,000 GMP cleanrooms covering lyophilization, filling, gel & dressing lines
Standard purification workshop
Registration Support
110+ medical device registration certificates and full cosmetic filing support
Manufacturing only, no registration support
R&D Strength
72 invention patents, 30+ international patents, clinical data backing
Mainly formula-library replication
Sampling Capability
7–14 day custom sampling with formula confidentiality
Standard products mainly, long custom lead time
Category Coverage
Cosmetics, Class II/III medical devices & injectable aesthetics — full chain
Single category

Process

How We Work

Six standardized steps from idea to market, fully under control.

01

Requirement Discovery

Define product type, specs, quantity, target market and compliance.

02

Formulation & Sampling

R&D team develops custom formulas and provides samples for review.

03

Confirmation & Quote

Confirm formula, packaging & MOQ, sign cooperation agreement.

04

Mass Production & QC

Produce under GMP with full quality monitoring throughout.

05

Filling & Labeling

Filling, packaging and private-label per brand requirements.

06

Delivery & Release

Outgoing inspection, compliance documentation and logistics.

Packaging

Packaging Options

Multiple packaging formats with full customization.

Bottle

瓶

Tube

管

Jar

罐

Ampoule

安瓿

Lyophilized Dual-Chamber

冻干双腔

Mask Sachet

面膜袋

FAQ

FAQ

Everything you may want to know about manufacturing, sampling and compliance.

What is your minimum order quantity (MOQ)?+

MOQ varies by product. Medical gels and dressings generally start from 10,000 units, while skin care can be lower. It depends on the product and formula—please contact us for a quote.

What certifications does Weitai Group hold?+

Weitai Group is fully qualified: certified with ISO13485 (medical device quality management) and ISO22716/GMPC (cosmetics GMP), recognized as a National High-Tech Enterprise, and certified with GB/T29490 IP management system. We hold 110+ Class II medical device registrations, 72 invention patents and 30+ international patents, operate 100,000-class GMP cleanrooms across six production bases totaling 150,000 m² with 65 automated production lines, and bring 25+ years of OEM/ODM experience serving 1000+ partner brands.

What is the difference between ODM and OEM?+

OEM manufactures your existing formulas and machines under your brand; ODM offers full customization from formula development, packaging design to registration. Weitai supports both and provides free formula development and documentation kits.

Can you provide formula development?+

Yes. With a 105-person R&D team, Weitai offers free formula development, packaging design, and documentation kits (brochures, detail pages, test reports) plus assistance with registration.

How can I get a quote?+

Please submit your product requirements and quantities via the inquiry form or sales@zhenmeifu.com. Our dedicated sales will contact you within 24 hours with a proposal and quotation.

Can you provide OEM/ODM contract manufacturing for PLLA microsphere injectable fillers?+

Yes. Weitai supports OEM/ODM contract manufacturing for Class III Medical Device injectable filler products, including PLLA microsphere injectable fillers. The microspheres feature uniform and controllable particle size and are biodegradable, with customizable formulations and aseptic filling available.

Turn your product idea into reality

Bring your product idea to a reliable partner — from formula and sample to mass production, Weitai walks with you end to end.