Not currently registered with FDA under this name

Exel Intl.

Culver City, CA, United States. Named as applicant on 1 dental 510(k) clearance between 1986 and 1986. No establishment is registered with FDA under this exact name today.

Device types listed: 0
Brands and models: 0
510(k) clearances: 11986–1986
Markets registered in: 1United States
Establishments: 0—

510(k) clearances per year, 1980–2026

510(k) clearances

Clearances on which FDA names Exel Intl. as the applicant.

Decided	510(k)	Device	Device type
11 Apr 1986	K861150	EXEL DENTAL NEEDLE	DZM Dental Needle

Some of these clearances are listed with FDA today by another company: Exelint International Co (1), Nipro Corporation (1).

Sources

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 of the most recent filing, which can be a US agent.