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Quick Answer Choosing a tampon manufacturer in China requires verifying certifications, quality control systems, traceability, production capacity, and communication reliability.EU and US buyers should always request samples, documentation packs, and packaging capabilities before placing bulk OEM or private label orders. TL;DR (Key Buyer Takeaways) 1. Why Many EU/US Brands Source Tampons from China China-based OEM […]

Quick Answer Tampons are regulated in the United States, and importers must ensure their products meet FDA-related compliance expectations. For private label tampon buyers, the most important step is to work with an OEM manufacturer that can provide a complete documentation package, including product specifications, quality records, and labeling support. This guide is for informational

Quick Answer If you are looking for a private label tampon manufacturer, MOQ (minimum order quantity), lead time, and pricing mainly depend on three factors: product type (organic or conventional), applicator requirements, and packaging customization. Most first-time buyers can reduce risk by starting with standard sizes and packaging, then scaling into fully customized branding once

Key Differences, Costs & Compliance Explained Quick Answer OEM tampon manufacturing involves producing tampons based on a brand’s custom specifications, while private label manufacturing uses pre-developed tampon designs branded under a buyer’s name. Both models must meet FDA medical device regulations, but OEM offers greater customization and brand differentiation. What Is OEM Tampon Manufacturing? OEM

FDA Standards, Testing Methods & Labeling Guide Quick Answer Tampon absorbency levels are regulated by the FDA and must be classified according to standardized absorbency ranges measured in grams. Manufacturers are required to test absorbency using approved methods and label tampons accurately to help reduce the risk of Toxic Shock Syndrome (TSS). What Are Tampon

What Tampon Manufacturers Must Know Quick Answer ISO 13485 is an international quality management standard for medical device manufacturers. For tampon manufacturers, ISO 13485 demonstrates compliance with the FDA Quality System Regulation (21 CFR Part 820) by ensuring controlled production, traceability, risk management, and consistent product safety. What Is ISO 13485? ISO 13485 is a

Complete Compliance Guide for OEM & Private Label Brands Quick Answer Tampon manufacturers exporting to the United States must comply with FDA medical device regulations, including facility registration, device listing, Quality System Regulation (21 CFR Part 820), proper labeling, and post-market surveillance. Tampons are classified as Class II medical devices by the FDA. Are Tampons

FDA, ISO & OEM Checklist for Private Label Brands Quick Answer A reliable tampon manufacturer should be FDA-registered, ISO 13485 certified, and capable of private label OEM production with strict quality control, independent lab testing, and transparent manufacturing processes. Why Choosing the Right Tampon Manufacturer Matters Tampons are medical-grade feminine hygiene products. Choosing the wrong

When choosing tampons, many people wonder whether organic cotton tampons are actually different from regular ones—or if it’s just a marketing term. The short answer:The difference isn’t about absorbency—it’s about materials, additives, and personal comfort. If you’re curious to try organic cotton for yourself, ready-to-ship personal packs are available here:https://tamponmanufacturer.com/organic-cotton-tampons-manufacturer/#for-personal-use What Are Regular Tampons Made

Short answer:For most people, using a tampon should not hurt. Discomfort usually comes from choosing the wrong absorbency, incorrect insertion angle, or feeling tense—especially the first time. If you’re curious but a bit nervous, starting with a small personal pack of Regular absorbency can help you try at your own pace.→ Ready-to-ship organic cotton tampons