Manufacturer registered with FDA

3D LifePrints UK

Liverpool, United Kingdom. Lists 1 dental device type with FDA across 2 registered establishments, and holds 1 510(k) clearance as applicant.

FDA owner/operator10085716Contract manufacturerManufacturer1 clearance in five years

Device types listed: 1
Brands and models: 1
510(k) clearances: 12022–2022
Markets registered in: 1United States
Establishments: 2United States

510(k) clearances per year, 2007–2026

Devices listed with FDA

What 3D LifePrints UK currently lists, by FDA device type, with the brand and model names on the listing.

Device type	Category	Role	Brands and models	Listed since
Manual Wire Driver and Bone DrillDZJ · Class 2	Surgical drills & motors	Maker	EmbedMed	2023

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

510(k) clearances

Clearances on which FDA names 3D LifePrints UK as the applicant, including filings under its other names.

Decided	510(k)	Device	Device type
30 Sep 2022	K220366	EmbedMed	DZJ Manual Wire Driver and Bone Drill

Registered establishments

Establishment	Location	What it does
Insight Surgery HoustonFDA reg. 3027329005	Houston, TX, United States	Manufacturer
Insight Surgery NebraskaFDA reg. 3038011206	Omaha, NE, United States	Contract manufacturer

Other names on FDA records

Insight Surgery Houston · Insight Surgery Nebraska

Sources

FDA establishment registration & device listing (search FDA, owner/operator 10085716). 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.