Trublend® SLM® 0 Deg. Posteriors

144 catalogue numbers from T13 U 433, listed by Dentsply LLC, United States, under Denture, Plastic, Teeth. 26 manufacturers in China are registered for this product code.

Registry build 21.09.26
26manufacturers in China registered for this device type
144catalogue numbers in this listing
4510(k) clearances naming this product code

Who Else Makes It

Concentrated in Guangdong (11), Jiangsu (3), Hong Kong (3). One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code ELM
Manufacturer City Province Registered as Device types
Shenzhen Jiahong Dental Technology Co., Ltd. Shenzhen Guangdong Contract manufacturer 7
Debo Medical Technology (Shijiazhuang) Co., Ltd. Shijiazhuang Hebei Contract manufacturer 117
Wuxi Lyusmile IMP AND EXP Co., Ltd. Wuxi Jiangsu Private-label distributor 66
Dongguan Wanjin Industrial Co., Ltd. Dongguang Guangdong Remanufacturer 41
Fuzhou Delphin BIO-Tech Co., Ltd. Fuzhou Fujian Manufacturer 18
Shandong Huge Dental Material Corporation Rizhao Shandong Manufacturer 17
Shenzhen Sunmc Dental Technology Co., Ltd. Shenzhen Guangdong Manufacturer 17
Improve Co., Limited Lantau Island Hong Kong Contract manufacturer 16
Shanghai Fanta Dental Materials Co., Ltd. Shanghai Shanghai Manufacturer 15
Heyuan HEY White Technology Co., Ltd. Heyuan Guangdong Manufacturer 12
Beijing Yingguan Dental Science&Technology Co., Ltd. Beijing Beijing Manufacturer 11
Smile Dental Laboratory Company Limited Zhuhai Guangdong Manufacturer 11

Showing 12 of 26. All 26 manufacturers in China registered for Denture, Plastic, Teeth

Record

Regulatory record for Trublend® SLM® 0 Deg. Posteriors
Listed by Dentsply LLC, United States
FDA product code ELM
Device type Denture, Plastic, Teeth
Device class Class 2
Regulation 21 CFR 872.3590
Establishment Contract manufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
Record published 2016-10-10
Record revised 2023-12-13 (version 5)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Single use Yes
Prescription Prescription only
Label carries lot or batch number
Distribution end date 2022-06-01

Catalogue Numbers

Catalogue numbers for Trublend® SLM® 0 Deg. Posteriors
Catalogue number Size Status
T13 U 433 Withdrawn
T15 L 433 Withdrawn
T02 L 429 Withdrawn
T17 L 433 Withdrawn
T08 U 433 Withdrawn
T14 L 429 Withdrawn
T23 L 429 Withdrawn
T12 U 433 Withdrawn
T16 L 431 Withdrawn
T07 U 429 Withdrawn
T21 U 433 Withdrawn
T05 U 431 Withdrawn
T15 U 429 Withdrawn
T08 L 433 Withdrawn
T01 U 433 Withdrawn
T04 L 433 Withdrawn
T20 L 429 Withdrawn
T13 L 431 Withdrawn
T23 U 431 Withdrawn
T04 U 429 Withdrawn
T24 L 431 Withdrawn
T06 L 431 Withdrawn
T23 L 433 Withdrawn
T07 U 431 Withdrawn
T23 U 433 Withdrawn
T14 U 431 Withdrawn
T10 L 433 Withdrawn
T24 U 431 Withdrawn
T02 U 433 Withdrawn
T10 U 431 Withdrawn
T19 U 431 Withdrawn
T08 U 429 Withdrawn
T23 L 431 Withdrawn
T19 L 431 Withdrawn
T05 L 429 Withdrawn
T07 L 433 Withdrawn
T01 U 429 Withdrawn
T03 U 429 Withdrawn
T17 U 429 Withdrawn
T17 U 431 Withdrawn
T02 L 431 Withdrawn
T17 L 431 Withdrawn
T09 L 429 Withdrawn
T03 L 433 Withdrawn
T21 L 429 Withdrawn
T10 U 433 Withdrawn
T06 L 429 Withdrawn
T01 U 431 Withdrawn
T14 L 431 Withdrawn
T11 U 433 Withdrawn
T03 L 429 Withdrawn
T08 U 431 Withdrawn
T05 U 429 Withdrawn
T08 L 431 Withdrawn
T14 L 433 Withdrawn
T24 L 433 Withdrawn
T05 L 433 Withdrawn
T16 U 431 Withdrawn
T01 L 431 Withdrawn
T11 U 429 Withdrawn
T04 U 433 Withdrawn
T17 U 433 Withdrawn
T18 U 431 Withdrawn
T12 U 431 Withdrawn
T06 U 431 Withdrawn
T23 U 429 Withdrawn
T03 U 431 Withdrawn
T07 L 429 Withdrawn
T07 U 433 Withdrawn
T22 L 433 Withdrawn
T04 L 429 Withdrawn
T13 L 429 Withdrawn
T10 L 431 Withdrawn
T10 U 429 Withdrawn
T14 U 433 Withdrawn
T11 L 431 Withdrawn
T08 L 429 Withdrawn
T09 L 433 Withdrawn
T18 L 433 Withdrawn
T07 L 431 Withdrawn
T05 U 433 Withdrawn
T11 L 433 Withdrawn
T19 U 433 Withdrawn
T19 L 433 Withdrawn
T19 U 429 Withdrawn
T01 L 429 Withdrawn
T12 L 431 Withdrawn
T22 U 429 Withdrawn
T24 L 429 Withdrawn
T21 U 431 Withdrawn
T24 U 429 Withdrawn
T20 L 431 Withdrawn
T10 L 429 Withdrawn
T22 L 431 Withdrawn
T15 U 433 Withdrawn
T18 U 429 Withdrawn
T22 U 431 Withdrawn
T18 L 431 Withdrawn
T09 U 433 Withdrawn
T15 L 431 Withdrawn
T12 U 429 Withdrawn
T13 L 433 Withdrawn
T06 U 429 Withdrawn
T16 U 429 Withdrawn
T17 L 429 Withdrawn
T16 U 433 Withdrawn
T14 U 429 Withdrawn
T22 L 429 Withdrawn
T13 U 431 Withdrawn
T18 L 429 Withdrawn
T06 L 433 Withdrawn
T11 U 431 Withdrawn
T21 U 429 Withdrawn
T11 L 429 Withdrawn
T05 L 431 Withdrawn
T20 U 431 Withdrawn
T12 L 429 Withdrawn
T15 U 431 Withdrawn
T04 L 431 Withdrawn
T02 L 433 Withdrawn
T21 L 431 Withdrawn
T03 L 431 Withdrawn
T09 U 429 Withdrawn
T09 L 431 Withdrawn
T16 L 429 Withdrawn
T19 L 429 Withdrawn
T03 U 433 Withdrawn
T12 L 433 Withdrawn
T16 L 433 Withdrawn
T22 U 433 Withdrawn
T20 U 433 Withdrawn
T04 U 431 Withdrawn
T01 L 433 Withdrawn
T20 L 433 Withdrawn
T24 U 433 Withdrawn
T09 U 431 Withdrawn
T13 U 429 Withdrawn
T06 U 433 Withdrawn
T15 L 429 Withdrawn
T18 U 433 Withdrawn
T02 U 431 Withdrawn
T02 U 429 Withdrawn
T20 U 429 Withdrawn
T21 L 433 Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Resin Teeth DCL PE Ivoclar Vivadent Aktiengesellschaft 8,657
Primodent Polident d.o.o. 3,814
Resin Teeth S PE S DCL Ivoclar Vivadent Aktiengesellschaft 2,870
Vitapan Vita – Zahnfabrik H. Rauter Gesellschaft mit beschränkter Haftung & Co Kommanditgesellschaft 2,480
Myerson Special The Myerson Company Limited 2,386
Kenson The Myerson Company Limited 2,365
Candulor TCR Candulor, AG 1,944
Vita Physiodens Vita – Zahnfabrik H. Rauter Gesellschaft mit beschränkter Haftung & Co Kommanditgesellschaft 1,788
Portrait® IPN® Anteriors Dentsply LLC 1,674
Enigma Denture Teeth – Pairs Davis Schottlander & Davis, Ltd. 1,632
Ivostar Gnathostar Ivoclar Vivadent Aktiengesellschaft 1,501
REF-Line Polident d.o.o. 1,458

Showing 12 of 9,979. All products under Denture, Plastic, Teeth

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K920684 1992-12-23
K831214 1983-05-09
K792245 1980-01-04
K780217 1978-03-15

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