Tool · 510(k)

510(k) Predicate Finder

Find potential predicate devices for your 510(k) submission. Enter a K-number to find all clearances with the same product code, a three-letter product code to browse clearances directly, or search by device name.

Product Code: DZL FDA class 2

Screw, Fixation, Intraosseous

Dental

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The Intraosseous Fixation Screw is a dental and oral surgical implant inserted into bone to stabilize jaw fractures, secure osteotomy segments, or anchor bone grafts during oral and maxillofacial surgical procedures. It is classified as FDA Class 2, indicating moderate risk, and requires 510(k) clearance before marketing. The product code is DZL and the applicable regulation is 21 CFR 872.4880, under the Dental medical specialty. This device is an implant.

510(k) Clearances

50+ matches
K Number
Device Name
USTOMED Bone Fixation/Bone Augmentation Systems - PIN
GBR System
MP Pin flat without thread (36BMP000020/MP20)
KLS Martin Drill-Free MMF Screw
Stryker MP, Mandible, HMMF and MMF AXS Screws
SAVE GBR
The Micro Screw System, Micro Screw System Basic
Membrane Screws and Membrane Tacks
Bone Screw, Bone Tack
OssBuilder System
Intra-Lock Bone Fixation System
Salvin Tenting Screw System
Neo GBR System
MC BIO Supertack Tack 3mm, 4mm and 5mm
OsteoMed IMF Screw
JUGGERKNOT MINI SOFT ANCHOR
DENTAL BONE SCREWS; DENTAL BONE SCREWS, CONTINUING; SCREW SYSTEM TX; SCREW SYSTEM TX PROFESSIONAL
MEISINGER TACS (MEISINGER MEITAC-KIT), MEISINGER PINS (MEISINGER MASTER-PIN-CONTROL-KIT, BASIC-KIT
NEODENT GRAFT SCREW
J TAC MODEL JT-MD-035, JT-MD-040, JT-MD-045, JT-CL-030
SALVIN DENTAL SPECIALTIES FIXATION SCREW
PRO-FIX PRECISION FIXATION SYSTEM MODEL PFM#, PFB#, PFT#
RAPIDSORB PLUS SCREW SYSTEM
MILTEX MEMBRANE TACK KIT
DRILL FREE MMF SCREW
STOMA BONE BLOCK SCREW
SALVIN DENTAL SPECIALTIES, INC., FIXATION SCREW
ALPHA BIO BONE FIXATION SCREW SYSTEM
STOMA BONE SCREW
SYNTHES 1.0MM TI. CORTEX, SELF-DRILLING SCREWS (CARNIOFACIAL)
BONE BLOCK FIXATION SET
STRYKER MMF SCREW
KLS MARTIN DRILL-FREE MMF SCREW
SYNTHES (USA) 1.0/1.22 MM CRANIOFACIAL SCREWS
SYNTHES LOW PROFILE NEURO SYSTEM - 3 MM SCREWS
THE AUTOTAC SYSTEM TITANIUM TACK
SYNTHES (USA) 1.3 MM CRANIOFACIAL SCREWS
LORENZ 1.5 X 4 MM LACTOSORB TAP FREE SCREW
OSTEOMED BIORESORBABLE FIXATION SYSTEM
BIOPLATE RESORBABLE BONE SCREW
THE AUTOTAC SYSTEM
SYNTHES TITANIUM MULTI-VECTOR DISTRACTOR
SYNTHES (USA) IMF SCREWS
SYNTHES 1.5MM TI BROW LIFT SCREW
LACTOSORB PUSH SCREW
THE AUTOTAC SYSTEM
RESOLVE QUICKANCHOR
KLS-MARTIN MMF SCREW
TALON ANCHOR SNAP-PAK
MITEK MINI ANCHOR

What is a Predicate Device?

A predicate device is a legally marketed device that a new 510(k) applicant uses to demonstrate substantial equivalence. The FDA's 510(k) pathway requires manufacturers to show that their device has the same intended use and similar technological characteristics as one or more predicate devices already cleared for commercial distribution.

Finding the right predicate is a critical step in 510(k) strategy. Manufacturers typically search for cleared devices with the same FDA product code, which groups devices by their intended use and regulatory classification. This tool helps you identify potential predicates by browsing all clearances within a product code.

Note that predicate devices must be legally marketed — they cannot be devices that were cleared but never commercialized, or devices subject to a mandatory recall. The determination of substantial equivalence considers intended use, technological characteristics, and performance data.

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