Premier Cavity Prep

CPI Carver-Black DE_BC 89/92

Registry build 21.09.26
5manufacturers in China registered for this device type
1catalogue number
1510(k) clearance

Who Else Makes It

Concentrated in Shanghai (4), Shandong (1).

Chinese manufacturers registered for FDA product code EKH
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
Shanghai Kangqiao Dental Instruments Factory Shanghai Shanghai Manufacturer 54
Shanghai Dochem Industries Co., Ltd. Shanghai Shanghai Manufacturer 45
Shanghai Smedent Medical Instrument Co., Ltd. Shanghai Shanghai Repacker / relabeller 30

Record

Regulatory record for Premier Cavity Prep
Listed by Premier Dental Products Co., United States
FDA product code EKH
Device type Carver, Dental Amalgam, Operative
Device class Class 1
Regulation 21 CFR 872.4565
Establishment Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer
Premarket notification Exempt
Record published 2026-04-01

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, manufacturing date

Catalogue Numbers

Catalogue numbers for Premier Cavity Prep
Catalogue number Size Status
1003240 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
HU-Friedy HU-Friedy MFG Co., LLC 284
Nordent Manufacturing Inc Nordent Manufacturing Inc 154
American Eagle Instruments American Eagle Instruments 72
Zoll-Dental Zoll-Dental 43
Power Dental USA Power Dental U.S.A. Inc. 39
A. Titan Instruments A. Titan Instruments, Inc. 38
Sklar® Sklar Corporation 33
Integra® Miltex® Integra LifeSciences Production Corporation 29
Reicodent Devemed Gmbh 29
Premier Carvers Premier Dental Products Co. 20
J & J Instruments Inc J & J Instruments, LLC 20
devemed Devemed Gmbh 16

Showing 12 of 41. All products under Carver, Dental Amalgam, Operative

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K780528 1978-04-19

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