Manufacturer registered with FDA

Inman Orthodontic Laboratories, Inc.

Coral Springs, FL, United States. Lists 2 dental device types with FDA across 1 registered establishment, and holds 1 510(k) clearance as applicant.

FDA owner/operator9085140ManufacturerSpecification developer

Device types listed: 2
Brands and models: 2
510(k) clearances: 12021–2021
Markets registered in: 1United States
Establishments: 1United States

510(k) clearances per year, 2007–2026

Devices listed with FDA

What Inman Orthodontic Laboratories, Inc. currently lists, by FDA device type, with the brand and model names on the listing.

Device type	Category	Role	Brands and models	Listed since
Orthodontic Wire ClampECN · Class 1	—	Maker	INMAN POWER COMPONENT	2006
Sequential AlignerNXC · Class 2	Clear aligners	Maker	Digital Clear Aligners (DCAs)	2021

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 Inman Orthodontic Laboratories, Inc. as the applicant.

Decided	510(k)	Device	Device type
29 Sep 2021	K210763	Inman Digital Clear Aligners	NXC Sequential Aligner

Registered establishments

Establishment	Location	What it does
INMAN ORTHODONTIC LABORATORIES, INC.FDA reg. 3005663102	CORAL SPRINGS, FL, United States	Manufacturer, Specification developer

Sources

FDA establishment registration & device listing (search FDA, owner/operator 9085140). 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.