Manufacturer registered with FDA

Span Packaging Services LLC dba Multi-Pack Solutions

Greenville, SC, United States. Lists 2 dental device types with FDA across 1 registered establishment.

FDA owner/operator9033516Contract manufacturer
Device types listed
2
Brands and models
0
510(k) clearances
0as applicant
Markets registered in
36 registrations outside the US
Establishments
1United States

Registered in 3 markets

Where regulators' registries name Span Packaging Services LLC dba Multi-Pack Solutions as the manufacturer or the registration holder of a device.

All markets
United States: 2 device types listedTaiwan: 5 registrationsSouth Korea: 1 registrations
RegisteredHome: United StatesOne marker per market
MarketRegulatorNamed asName on the registryRegistrationsIssuedRecords
United StatesFDAManufacturerSpan Packaging Services LLC dba Multi-Pack Solutions2 device types—Below
TaiwanTFDAManufacturerSPAN Packaging Services LLC. d/b/a Multi-Pack Solutions52016–2018Pure Global AI
South KoreaMFDSManufacturerSpan Packaging Services, LLC d/b/a Multi-Pack Solutions12015–2015Pure Global AI

Outside the US the count is of all the company's device registrations in that market, dental or not · matched by company name and country · registry data read 12 Nov 2026

Devices listed with FDA

What Span Packaging Services LLC dba Multi-Pack Solutions currently lists, by FDA device type, with the brand and model names on the listing.

Device typeCategoryRoleBrands and modelsListed since
Dental Rapid Wax ApplicatorEIT · Class 2—Maker—2013
Oral Cavity Abrasive Polishing AgentEJR · Class 1Polishing & prophylaxisMaker—2005

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

Registered establishments

EstablishmentLocationWhat it does
SPAN PACKAGING SERVICES d.b.a. MULTI-PACK SOLUTIONSFDA reg. 1063707Greenville, SC, United StatesContract manufacturer

Other names on FDA records

SPAN PACKAGING SERVICES d.b.a. MULTI-PACK SOLUTIONS

Sources

FDA establishment registration & device listing (search FDA, owner/operator 9033516). 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.