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10 de agosto de 2026

Implant Neobiocare Nobel Screwdrivers HEX Hand Driver Torque Wrench Adapter ICM

Universal Implant Prosthetic Kit Drivers Manual HEX 1.2mm Neobiocare Ratchet Torque Wrench 3I. GSM Implant Prosthetic Universal Kit. Totally 16 drivers, compatible with different implant system. Torque Wrench Ratchet (15-70Ncm).
10 de agosto de 2026

Implant Screwdriver Drivers Torque Wrench Adapter Hex 1.2mm Biomet 3I Osstem DIO

Dental Implant Screwdriver Hex 1.2 Kit Torque Wrench Hand Latch Driver Osstem 3I. Adapter to connect the latch Screwdriver to the Manual or Torque Wrench Prosthetic. Manual Torque Wrench Adapter. Torque Wrench.
10 de agosto de 2026

Implant Screwdriver Angulated Screw Channel 1.2 Hiossen Osstem Biomet 3i Megagen

Ratchet screwdriver for Angulated Screw Channel. For hand use or torque wrench ratchet with a 7mm hole like dentium straumann. The sale of this item may be subject to regulation by the U.S. Food and Drug Administration and state and local regulatory agencies.
10 de agosto de 2026

SURGICAL AUTOCLAVE STERILIZATION CASSETTES RACKS BOX FOR 5/10/20 INSTRUMENTS

FDA for Curing Light: 510(K) Number: K192233, Regulation Number: 21 CFR 872.6070, Product Code: EBZ. FDA for Handpiece: 510(K) Number: K181691, Regulation Number: 872.4200, Classification Product Code: EFB, Subsequent Product Code: EGS.
10 de agosto de 2026

Instruments Sterilization Box for 5/10/20 Surgical Dental Sterilizing Instrument

FDA for Curing Light: 510(K) Number: K192233, Regulation Number: 21 CFR 872.6070, Product Code: EBZ. FDA for Handpiece: 510(K) Number: K181691, Regulation Number: 872.4200, Classification Product Code: EFB, Subsequent Product Code: EGS.
10 de agosto de 2026

10 DENTAL SURGICAL AUTOCLAVE STERILIZATION CASSETTE BOX FOR 5 INSTRUMENTS

FDA for Curing Light: 510(K) Number: K192233, Regulation Number: 21 CFR 872.6070, Product Code: EBZ. FDA for Handpiece: 510(K) Number: K181691, Regulation Number: 872.4200, Classification Product Code: EFB, Subsequent Product Code: EGS.
10 de agosto de 2026

10 DENTAL SURGICAL AUTOCLAVE STERILIZATION CASSETTE BOX FOR 5 INSTRUMENTS

FDA for Curing Light: 510(K) Number: K192233, Regulation Number: 21 CFR 872.6070, Product Code: EBZ. FDA for Handpiece: 510(K) Number: K181691, Regulation Number: 872.4200, Classification Product Code: EFB, Subsequent Product Code: EGS.
10 de agosto de 2026

1-10 DENTAL AUTOCLAVE STERILIZATION CASSETTE RACK BOX TRAY FOR 5 INSTRUMENTS

FDA for Curing Light: 510(K) Number: K192233, Regulation Number: 21 CFR 872.6070, Product Code: EBZ. The sale of this item may be subject to regulation by the U.S. Food and Drug Administration and state and local regulatory agencies.
10 de agosto de 2026

Dental Cassette Tray Sterilization Box Autoclave Surgical for 5 Instruments

The sale of this item may be subject to regulation by the U.S. Food and Drug Administration and state and local regulatory agencies. FDA for Curing Light: 510(K) Number: K192233, Regulation Number: 21 CFR 872.6070, Product Code: EBZ.
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