DZL
THE AUTOTAC SYSTEM
- Advisory panel
- Dental
- Total cleared
- 80
Adverse events under product code DZL
product code DZL- Injury
- 168
- Total
- 168
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Recent clearances under product code DZL
- K250123 — Master-Pin X (MP Pin with thread) (36BMP000030 / MP30)
- K251569 — Bone Screw
- K243190 — USTOMED Bone Fixation/Bone Augmentation Systems - PIN
- K233419 — GBR System
- K240321 — MP Pin flat without thread (36BMP000020/MP20)
- K233721 — KLS Martin Drill-Free MMF Screw
- K231599 — Stryker MP, Mandible, HMMF and MMF AXS Screws
- K222367 — SAVE GBR
- K201210 — The Micro Screw System, Micro Screw System Basic
- K201561 — Membrane Screws and Membrane Tacks
- K182881 — Bone Screw, Bone Tack
- K181854 — OssBuilder System
- K171831 — Intra-Lock Bone Fixation System
- K161857 — Salvin Tenting Screw System
- K160991 — Neo GBR System
- K151540 — MC BIO Supertack Tack 3mm, 4mm and 5mm
- K151195 — OsteoMed IMF Screw
- K140908 — JUGGERKNOT MINI SOFT ANCHOR
- K132212 — DENTAL BONE SCREWS; DENTAL BONE SCREWS, CONTINUING; SCREW SYSTEM TX; SCREW SYSTEM TX PROFESSIONAL
- K130682 — MEISINGER TACS (MEISINGER MEITAC-KIT), MEISINGER PINS (MEISINGER MASTER-PIN-CONTROL-KIT, BASIC-KIT
- K103084 — NEODENT GRAFT SCREW
- K101902 — J TAC MODEL JT-MD-035, JT-MD-040, JT-MD-045, JT-CL-030
- K100182 — SALVIN DENTAL SPECIALTIES FIXATION SCREW
- K093719 — PRO-FIX PRECISION FIXATION SYSTEM MODEL PFM#, PFB#, PFT#
- K093464 — RAPIDSORB PLUS SCREW SYSTEM
- K092855 — MILTEX MEMBRANE TACK KIT
- K083432 — DRILL FREE MMF SCREW
- K080430 — STOMA BONE BLOCK SCREW
- K073342 — SALVIN DENTAL SPECIALTIES, INC., FIXATION SCREW
- K063769 — ALPHA BIO BONE FIXATION SCREW SYSTEM
- K051871 — STOMA BONE SCREW
- K050606 — SYNTHES 1.0MM TI. CORTEX, SELF-DRILLING SCREWS (CARNIOFACIAL)
- K050515 — BONE BLOCK FIXATION SET
- K050535 — STRYKER MMF SCREW
- K042573 — KLS MARTIN DRILL-FREE MMF SCREW
- K041887 — SYNTHES (USA) 1.0/1.22 MM CRANIOFACIAL SCREWS
- K031807 — SYNTHES LOW PROFILE NEURO SYSTEM - 3 MM SCREWS
- K022790 — THE AUTOTAC SYSTEM TITANIUM TACK
- K021850 — SYNTHES (USA) 1.3 MM CRANIOFACIAL SCREWS
- K021522 — LORENZ 1.5 X 4 MM LACTOSORB TAP FREE SCREW
- K012486 — OSTEOMED BIORESORBABLE FIXATION SYSTEM
- K012908 — BIOPLATE RESORBABLE BONE SCREW
- K011675 — THE AUTOTAC SYSTEM
- K010690 — SYNTHES TITANIUM MULTI-VECTOR DISTRACTOR
- K010527 — SYNTHES (USA) IMF SCREWS
- K002935 — SYNTHES 1.5MM TI BROW LIFT SCREW
- K002423 — LACTOSORB PUSH SCREW
- K993493 — THE AUTOTAC SYSTEM
- K993575 — RESOLVE QUICKANCHOR
- K980760 — KLS-MARTIN MMF SCREW
- K993327 — TALON ANCHOR SNAP-PAK
- K992623 — MITEK MINI ANCHOR
- K982951 — IMTEC BIOPIN
- K983728 — LORENZ IMF SCREW
- K983485 — SYNTHES 1.3 MM SELF-DRILLING SCREW
- K981881 — DRG SHERLOCK MF BONE SCREW, COCRMO SELF-TAPPING, TI ALLOY SELF-TAPPING/SELF DRILLING, COCRMO SELF-TAPPING/ SELF DRILLING
- K981666 — 2.5 MM LACTOSORB SCREWS
- K982927 — QUICK TAP SELF DRILLING SCREW
- K981459 — MEMBRANE TACK
- K981362 — SYNTHES (USA) EXTERNAL MULTI VECTOR MANDIBLE DISTRACTOR
- K980199 — SYNTHES 1.5MM/2.0MM ORTHOGNATHIC MAXILLARY PLATES AND SCREWS
- K974817 — DRG MF TITANIUN ALLOY BONE SCREW 1.0MM, 1.2MM, 1.3MM, 1.5MM, 1.7MM, 2.0MM, 2.4MM
- K974392 — LEADFIX BIORESORBABLE MEMBRANCE PIN SYSTEM
- K972480 — 3I BIORESORBABLE FIXATION TACK
- K973180 — IMTEC BONE TAC
- K973056 — BONE GRAFT SCREW SYSTEM
- K962774 — OSTEOMED QUICKFIX
- K963546 — SMF TITANIUM (TI) ALLOY BONE SCREWS
- K964261 — SMF STAINLESS STEEL BONE SCREWS
- K961418 — OSTEOMED MSS
- K960945 — IMZ MEMBRANE TACK SYSTEM
- K955369 — MEMFIX
- K955140 — 2.0 X 6MM SCREW
- K952167 — IMZ BONE TACK SYSTEM
- K951510 — ACE BONE SCREW TACKING KIT
- K910427 — MEMFIX SCREWS
- K911936 — OSTEOMED SBF SYSTEM (SBF)
- K911165 — SCREW, BONE, MAXILLOFACIAL
- K770131 — LEW PROSTHETIC LOCKING DEVICE
- K761228 — LUHR MANDIBULAR COMPRESSION-SCREW SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.