Manufacturer registered with FDA
Maco Bag Corp.
Newark, NY, United States. Lists 1 dental device type with FDA across 1 registered establishment.
- Device types listed
- 1
- Brands and models
- 34
- 510(k) clearances
- 0as applicant
- Markets registered in
- 1United States
- Establishments
- 1United States
Devices listed with FDA
What Maco Bag Corp. currently lists, by FDA device type, with the brand and model names on the listing.
| Device type | Category | Role | Brands and models | Listed since |
|---|---|---|---|---|
| X-Ray Film HolderEGZ · Class 1 | — | Maker | Air Techniques 73066/2 Size 6Air Techniques 73248-0 Size 0Air Techniques 73248-1 Size 1Air Techniques 73248-2 Size 2Air Techniques 73248-2k Size 2 BulkAir Techniques 73248-3 Size 3Air Techniques 73248-4 Size 4Air Techniques A7395-2 Bite CoversDurr 0238-2130-070-01 Size 0 100/pkDurr 0238-2130-070-05 Size 0 Coex 100/pk 24 moreDurr 0238-2130-070-06 Size 0 NewDurr 0238-2130-071-01 Size 1 100/pkDurr 0238-2130-072-01 Size 2 300/pkDurr 0238-2130-072-04 Size 2 500 ClamshellDurr 0238-2130-072-06 Size 2 300/pk - New LabelsDurr 0238-2130-073-01 Size 3 100/pkDurr 0238-2130-074-01 Size 4 100/pkDurr 0238-2130-080-01 Size 0Durr 0238-2130-080-05 Size 0 CoexDurr 0238-2130-081-01 Size 1Durr 0238-2130-082-01 Size 2Durr 0238-2130-082-04 Size 2 BulkDurr 0238-2130-082-05 Size 2 CoexDurr 0238-2130-083-01 Size 3Durr 0238-2130-084-01 Size 4Durr 0238-2134-085-00 Size 5Durr 0238-2140-074-01 Size 4 New 100/pkDurr 0238-2207-010-01 Bite CoverDurr 2130107001 Size 0 0238-G8511-0Durr 2130107101 Size 1 0238-G8511-1Durr 2130107204 Size 2 0238-G8511-2Durr 2130107204 Size 2K 0238-G8511-2KDurr 2130107301 Size 3 0238-G8511-3Durr 2130107401 Size 4 0238-G8511-4 | 2019 |
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
| Establishment | Location | What it does |
|---|---|---|
| MACO BAG CORP.FDA reg. 3001468798 | Newark, NY, United States | Contract manufacturer |
Sources
FDA establishment registration & device listing (search FDA, owner/operator 1316093). 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.