Manufacturer registered with FDA

Wishbone

Flemalle, Belgium. Lists 1 dental device type with FDA across 1 registered establishment, and holds 2 510(k) clearances as applicant.

FDA owner/operator10084894Manufacturer1 clearance in five years

Device types listed: 1
Brands and models: 3
510(k) clearances: 22021–2026
Markets registered in: 1United States
Establishments: 1Belgium

510(k) clearances per year, 2007–2026

Devices listed with FDA

What Wishbone currently lists, by FDA device type, with the brand and model names on the listing.

Device type	Category	Role	Brands and models	Listed since
Animal Source Bone Grafting MaterialNPM · Class 2	Bone grafts & membranes	Maker	W-BoneWishbone HAWishbone HAE	2022

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 Wishbone as the applicant.

Decided	510(k)	Device	Device type
9 Oct 2026	K260096	Wishbone HAE	NPM Animal Source Bone Grafting Material
20 Aug 2021	K211551	Wishbone HA	NPM Animal Source Bone Grafting Material

Registered establishments

Establishment	Location	What it does
WISHBONEFDA reg. 3013171899	Flemalle Liege, Belgium	Manufacturer

Sources

FDA establishment registration & device listing (search FDA, owner/operator 10084894). 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.