Anctek Viet Nam Company Limited (contract manufacturer, Bien Hoa Dong Nai, VN): 3 new FDA device listings, incl. light based over the counter wrinkle reduction
Anctek Viet Nam Company Limited (Bien Hoa Dong Nai): 3 new FDA device listings, incl. light based over the counter wrinkle reduction. Its amount of 3 is above the median of 2 (77th percentile). Dated 79 days ago, it serves as a historical benchmark. Score 70/100. As of 2026-11-04, from openFDA device registration and listing endpoint (U.S. Food and Drug Administration).
Data as of · Compiled by Zalwin from openFDA device registration and listing endpoint (U.S. Food and Drug Administration)
amount: 3 · 77th percentile of 2,709 DeviceEstablishmentPulse records · 1.5x the median
Free preview: all 14 published fields of this record are shown below. Locked: 40 related VN DeviceEstablishmentPulse records and the 5-column CSV export.
| Field | Value |
|---|---|
| Establishment | Anctek Viet Nam Company Limited |
| Role | Contract manufacturer |
| Establishment types | Manufacture Medical Device for Another Party (Contract Manufacturer) |
| Location | Bien Hoa Dong Nai, VN |
| New listings | 3 |
| Devices | Light Based Over The Counter Wrinkle Reduction; Over-The-Counter Powered Light Based Laser For Acne |
| Product codes | OHS, OLP |
| Device classes | Class II |
| Medical specialties | General, Plastic Surgery |
| Brand names | Omnilux Contour Face 2 RT011; LED Light Therapy Mask-RT01 |
| First new listing | 2026-08-18 |
| Latest new listing | 2026-08-18 |
| FDA registration number | 3048086714 |
| Registration expires | 2026-12-31 |
| amount percentile | 77th of 2,709 (median 2, 1.5x median) |
| Peer records CSV (41 VN records) | 🔒 Click to unlock → |
| CRM-ready export with official source URLs | 🔒 Click to unlock → |
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CSV columns: Establishment · Role · New listings · Devices · Latest listing · official source URL
- Source agency: openFDA device registration and listing endpoint (U.S. Food and Drug Administration)
- Record date: 2026-08-18
- Data refreshed: 2026-11-04
- Refunds on request within 14 days
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LIVE PUBLIC DATA Source: openFDA device registration and listing endpoint (U.S. Food and Drug Administration) · Last refreshed: Wed, 04 Nov 2026 21:52:36 GMT
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Peer benchmark and outreach value: Anctek Viet Nam Company Limited and 41 VN peers
- VN DeviceEstablishmentPulse records like this one: 41
- Anctek Viet Nam Company Limited's amount: 77th percentile of 2,709 records
- Timing: Low: older than 30 days
- Estimated pipeline if you contact every VN peer: $8,200 (peers × rate × deal size; an estimate from your assumptions, not a forecast)
70 / 100 Score
- Contract manufacturer or sterilizer adding work.
- Class II or III devices: QMS and regulatory demands.
- Several new listings at once.
What is the DeviceEstablishmentPulse record for Anctek Viet Nam Company Limited in Bien Hoa Dong Nai?
Anctek Viet Nam Company Limited (Bien Hoa Dong Nai, VN), a contract manufacturer, added 3 FDA device listings on 2026-08-18.
How does Anctek Viet Nam Company Limited compare to other DeviceEstablishmentPulse records?
Its amount of 3 sits in the upper half (77th percentile) of 2,709 records; the median is 2. It is 79 days old; check the official source for later updates before acting. Its Score of 70/100 puts it among the stronger signals in this feed.
Anctek Viet Nam Company Limited vs. top 3 peers
| Organization | Location | Amount | Percentile | Record date |
|---|---|---|---|---|
| Anctek Viet Nam Company Limited | Bien Hoa Dong Nai, VN | 3 | 77th | 2026-08-18 |
| Tecomet Inc. | Wilmington, MA | 3 | 77th | 2026-10-15 |
| Bard Shannon Limited | Humacao, PR | 3 | 77th | 2026-10-14 |
| Orchid Orthopedic Solutions Oregon, Inc. | Oregon City, OR | 3 | 77th | 2026-10-05 |
Related records
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- Cook Medical LLC
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- Millstone Medical Outsourcing LLC.
- Karl Storz Endoscopy-America, Inc.
- Orchid Orthopedic Solutions Oregon, Inc.
- Philips Ultrasound LLC
- Zimmer, Inc.
DeviceEstablishmentPulse: Contract manufacturer DeviceEstablishmentPulse: Foreign establishment
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From the openFDA device registration and listing data, refreshed weekly. A listing shows a device an establishment says it makes or handles for the U.S. market; it is not FDA clearance or approval. Contact persons and street addresses are not stored. Verify in the FDA Establishment Registration and Device Listing database.