Manufacturer registered with FDA

Shenzhen Jie Bishi Technology Co., LTD

Shenzhen, China. Lists 7 dental device types with FDA across 1 registered establishment.

FDA owner/operator10092220Foreign exporterManufacturer
Device types listed
7
Brands and models
20
510(k) clearances
0as applicant
Markets registered in
1United States
Establishments
1China

Devices listed with FDA

What Shenzhen Jie Bishi Technology Co., LTD currently lists, by FDA device type, with the brand and model names on the listing.

Device typeCategoryRoleBrands and modelsListed since
Mouth MirrorEAX · Class 1Dental hand instrumentsMaker
dental mirrorOral endoscopyR60,R70,R80,R90,R10,R11,R12,R13,R14,R15,R16,R17,R18,R19,R20,R30,R40,R50401,402,403,408,406,I60,I70,I80,I90,I10,I11,I12,I13,I14,I15,I16,I17,I18,I19,I20
2024
Oral Irrigation UnitEFS · Class 1Oral irrigatorsMaker
D60,D80,D90,D10,D11,D12,D13,D14,D15,D16,D17,D18,D20,D30,D40,D50,D70Oral rinsing kitW98,W99,W100,W200,W300,C3 Pro,C5 Pro,C8 Pro,C9 Pro,C2SEwater pik
2024
Oral Cavity Abrasive Polishing AgentEJR · Class 1Polishing & prophylaxisMaker
P1,P2,P3,P4,P5,P6,P7,P8,P9,P10,P11,P12,P13,P14,P15,P16,P17,P18,P19,P20
2024
Periodontic ScalerEMN · Class 1Dental hand instrumentsMaker
T11,T11 Pro,T11 Pro+,T12 Pro,T10,T99,T100,T200,T300,T9,T10 Pro,T12 Plus,T13,T13 Pro,T12,T20,T15,T15pr0,T18,T18pr0,T19T19pr0,T22,T22proUltrasound tooth cleaning instrument
2024
Powered ToothbrushJEQ · Class 1ToothbrushesMaker
Electric toothbrushM13,M14,M15,M16,M17,M18,M19T8,T8HC,T8PLUS,T8PRO,T3,T3HC,T3PLUS,T3PRO,QY009,M10,P3,T1,T2,T4,T5,T6,T7,T9,M60,M70,M80,M90,M10,M20,M30,M40,M50,M11,M12
2024
Dental FlossJES · Class 1Floss & interdental cleanersMaker
Ultrasound water flossW98,W99,W100,W200,W300,C3 Pro,C5 Pro,C8 Pro,C9 Pro,C2SEC3,C3PRO,C5,C5PRO,C6,C6SE,C6SE-BT,C8,C10
2024
Plaque Disclosing AgentQJC · Class 1—Maker
Dental plaque removal agentT11,T11 Pro,T11 Pro+,T12 Pro,T10,T99,T100,T200,T300,T9,T10 Pro,T12 Plus,T13,T13 Pro,T12,T20,T15,T15pr0,T18,T18pr0,T19T19pr0,T22
2024

Source: FDA establishment registration & device listing, 510(k) and product classification files · FDA data as of 2 Nov 2026 · snapshot 12 Nov 2026

Registered establishments

EstablishmentLocationWhat it does
SHENZHEN JIE BISHI TECHNOLOGY CO., LTDFDA reg. 3034731361Shenzhen Guangdong, ChinaForeign exporter, Manufacturer

Sources

FDA establishment registration & device listing (search FDA, owner/operator 10092220). FDA 510(k) premarket notification file. FDA data as of 2 Nov 2026; snapshot 12 Nov 2026. The location shown is the address on FDA's record.