Frontal Sinus Curette

Frontal Sinus Curette Straight CUP

Registry build 21.09.26
1manufacturer
3catalogue numbers in this listing

Who Else Makes It

Registered in Shanghai.

Chinese manufacturers registered for FDA product code KAP
Manufacturer City Province Registered as Device types
Shanghai Medical Instruments (Group) Ltd. Corp. Shanghai Shanghai Contract manufacturer 235

Record

Regulatory record for Frontal Sinus Curette
Listed by Sontec Instruments, Inc., United States
FDA product code KAP
Device type Curette, Nasal
Device class Class 1
Regulation 21 CFR 874.4420
Establishment Repacker / relabeller
Premarket notification Exempt
Record published 2018-09-13
Record revised 2026-03-05 (version 2)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Dry Heat Sterilization, Moist Heat or Steam Sterilization
Prescription Prescription only
Label carries lot or batch number
Sizes Length 7.5 in

Catalogue Numbers

Catalogue numbers for Frontal Sinus Curette
Catalogue number Size Status
320-771 Length 7.5 in In distribution
320-769 Length 7.5 in In distribution
320-770 Length 7.5 in In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
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V. Mueller Steris Corporation 20
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Sklar Sklar Corporation 19
Novo Surgical Novo Surgical, Inc. 18
Novo Surgical Inc. Novo Surgical, Inc. 16
Curette KLS-Martin L.P. 15
Jedmed Jedmed Instrument Company 14
MicroFrance® Integra Microfrance SAS 13

Showing 12 of 40. All products under Curette, Nasal

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

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