Fentex

Frontal Sinus Seeker by Kuhn double-ended, both sides curved 90° 22 cm, Fig. 2

Registry build 21.09.26
3manufacturers in China registered for this device type
52catalogue numbers in this listing

Who Else Makes It

Concentrated in Shanghai (1), Shandong (1), Zhejiang (1).

Chinese manufacturers registered for FDA product code KAK
Manufacturer City Province Registered as Device types
Shanghai Medical Instruments (Group) Ltd. Corp. Shanghai Shanghai Contract manufacturer 235
Xinhua Surgical Instrument Co., Ltd. Zibo Shandong Manufacturer 222
Hangzhou Haizhu MIM Products Co., Ltd. Hangzhou Zhejiang Exporter 28

Record

Regulatory record for Fentex
Listed by Fentex medical GmbH
FDA product code KAK
Device type Probe, Ent
Device class Class 1
Regulation 21 CFR 874.4420
Premarket notification Exempt
Record published 2022-12-08
Record revised 2026-07-20 (version 3)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Prescription Prescription only
Label carries lot or batch number
Distribution end date 2026-06-30

Catalogue Numbers

Catalogue numbers for Fentex
Catalogue number Size Status
156660FX In distribution
156635FX In distribution
163304FX In distribution
156650FX In distribution
443543FX In distribution
443528FX In distribution
418826FX In distribution
443520FX In distribution
156665FX In distribution
443522FX In distribution
156645FX In distribution
163306FX In distribution
418825FX In distribution
443541FX In distribution
443540FX In distribution
443546FX In distribution
021300FX In distribution
156670FX In distribution
021200FX In distribution
088114FX In distribution
443526FX In distribution
418719FX In distribution
443548FX In distribution
163308FX In distribution
156600FX In distribution
443542FX In distribution
443524FX In distribution
156640FX In distribution
418830FX In distribution
463000FX In distribution
443544FX In distribution
443518FX Withdrawn
443521FX Withdrawn
443530FX Withdrawn
443516FX Withdrawn
443509FX Withdrawn
443538FX Withdrawn
443513FX Withdrawn
443514FX Withdrawn
443533FX Withdrawn
443512FX Withdrawn
443539FX Withdrawn
443536FX Withdrawn
021100FX Withdrawn
443532FX Withdrawn
443519FX Withdrawn
443531FX Withdrawn
443529FX Withdrawn
443511FX Withdrawn
443510FX Withdrawn
443523FX Withdrawn
443534FX Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
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Pilling Teleflex Medical LLC 20
HNM Medical HNM Stainless, LLC. 19
Ambler Surgical Ambler Surgical, LLC 18
Medicon Medicon eG. Chirurgiemechaniker-Genossenschaft 17
mytaMed Mytamed, Inc. 16
RZ Medizintechnik GmbH RZ Medizintechnik Gmbh 15
V. Mueller Steris Corporation 12
Bowman salivary duct probe Spiggle & Theis Medizintechnik Gmbh 11
Millennium Avalign Technologies, Inc. 10
MSI Precision Specialty Instruments MED Saver, Inc. 10
Avalign Avalign Technologies, Inc. 9

Showing 12 of 52. All products under Probe, Ent

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