A Randomized Post-market Study to Evaluate Zip Device Compared to Sutures for Laceration Repair in Pediatrics and Adults

Inclusion Criteria: 1. Between 4 and above at the time of laceration repair. 2. Require suture closure as standard of care for simple straight wounds on trunk, extremities or face. 3. Low Tension Laceration, e.g. skin can be easily approximated by pinching with fingers. 4. Subject and legal representative(s) (if a pediatric subject) are willing and able to comply with the investigational device removal and meet the follow up requirements. 5. Subject and legal representative(s) (if a pediatric subject) have been informed of the nature, the scope and the relevance of the study. 6. Subject and legal representative(s) (if a pediatric subject) have voluntarily agreed to participation and have duly signed the Informed Consent Form. Exclusion Criteria: 1. Known personal or familial history of scar hypertrophy. 2. Known or suspected allergies or hypersensitivity to non-latex skin adhesives. 3. Atrophic skin deemed clinically prone to blistering. 4. Wounds that are easily susceptible to infection as a result of exposure to unsanitary conditions ("dirty wounds"). 5. Wounds that require deep dermal closure using sutures. 6. Known or suspected mental problems and/or aggressiveness that indicates that the subject might try to remove the device during the treatment period. 7. Ongoing treatment with cytostatic. 8. Known or suspected diagnosis of severe anorexia. 9. Participating in any other clinical investigation. 10. Known health condition that would affect healing in the opinion of the investigator. 11. Any subject that according to the Declaration of Helsinki is deemed unsuitable for study enrolment.