Manufacturer registered with FDA
Avilign Medical
Sialkot, Pakistan. Lists 11 dental device types with FDA across 1 registered establishment.
- Device types listed
- 11
- Brands and models
- 11
- 510(k) clearances
- 0as applicant
- Markets registered in
- 1United States
- Establishments
- 1Pakistan
Devices listed with FDA
What Avilign Medical currently lists, by FDA device type, with the brand and model names on the listing.
| Device type | Category | Role | Brands and models | Listed since |
|---|---|---|---|---|
| Irrigating (Dental) SyringeEIB · Class 1 | Dental hand instruments | Maker | Syringe, Irrigating (Dental) | 2020 |
| Crown RemoverEIS · Class 1 | Dental hand instruments | Maker | 72-10TC WYNMAN CROWN GRIPPER 6-1/4, TC, W/OUT RATCHET | 2026 |
| Endodontic Root Canal PluggerEKR · Class 1 | Dental hand instruments | Maker | Plugger, Root Canal, Endodontic | 2020 |
| Surgical HemostatEMD · Class 1 | Dental hand instruments | Maker | Hemostat Surgical | 2017 |
| Surgical Tooth Extractor ForcepsEMG · Class 1 | Dental hand instruments | Maker | FORCEPS TOOTH EXTRACTOR SURGICAL | 2017 |
| Surgical Rongeur ForcepsEMH · Class 1 | Dental hand instruments | Maker | Forceps, Rongeur, Surgical | 2020 |
| Dental Surgical ElevatorEMJ · Class 1 | Dental hand instruments | Maker | SELDIN PERIOSTEAL ELEVATOR 23, DOUBLE-ENDED | 2026 |
| Surgical Osteotome ChiselEMM · Class 1 | Dental hand instruments | Maker | CHISEL OSTEOTOME SURGICAL | 2017 |
| Periodontic ScalerEMN · Class 1 | Dental hand instruments | Maker | scalar | 2017 |
| Orthodontic PlierJEX · Class 1 | Dental hand instruments | Maker | PLIER, ORTHODONTIC | 2023 |
| FacebowKCR · Class 1 | Articulators & facebows | Maker | Facebow | 2020 |
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 |
|---|---|---|
| AVILIGN MEDICALFDA reg. 3012226300 | Sialkot Punjab, Pakistan | Contract manufacturer, Manufacturer, Repacker / relabeler |
Sources
FDA establishment registration & device listing (search FDA, owner/operator 10053881). 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.