Manufacturer registered with FDA

Richbolt Enterprises

SIALKOT, PUNJAB, Pakistan. Lists 14 dental device types with FDA across 1 registered establishment.

FDA owner/operator9002758Manufacturer
Device types listed
14
Brands and models
16
510(k) clearances
0as applicant
Markets registered in
1United States
Establishments
1Pakistan

Devices listed with FDA

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

Device typeCategoryRoleBrands and modelsListed since
Mouth MirrorEAX · Class 1Dental hand instrumentsMaker
RICHBOLT ENTERPRISES
2005
Resin Impression Tray MaterialEBH · Class 1Impression traysMaker
IMPRESSION TRAYS, S
2001
Orthodontic Bracket AlignerECQ · Class 1Dental hand instrumentsMaker
RICHBLOT ENTERPRISES
2005
Orthodontic Band PusherECS · Class 1Dental hand instrumentsMaker
RICHBOLT ENTERPRISES
2005
Dental Wax CarverEIK · Class 1Dental hand instrumentsMaker
RICHBOLT ENTERPRISES
2004
Crown RemoverEIS · Class 1Dental hand instrumentsMaker
RICHBOLT ENTERPRISES
2004
Periodontic ProbeEIX · Class 1Dental hand instrumentsMaker
RICHBOLT ENTERPRISES
2005
Operative Dental Amalgam CarverEKH · Class 1Dental hand instrumentsMaker
RICHBOLT ENTERPRISES
2005
Operative Amalgam CarrierEKI · Class 1Dental hand instrumentsMaker
RICHBOLT ENTERPRISES
2005
Surgical Tooth Extractor ForcepsEMG · Class 1Dental hand instrumentsMaker
RICHBOLT ENTERPRISES
2005
Periodontic ScalerEMN · Class 1Dental hand instrumentsMaker
SCALERS, S
2001
Matrix RetainerJEP · Class 1Dental hand instrumentsMaker
RICHBOLT ENTERPRISES
2004
Orthodontic PlierJEX · Class 1Dental hand instrumentsMaker
PLIERS ORTHODONTIC
1991
Preformed Tooth PositionerKMY · Class 1Retainers, expanders & headgearMaker
RICHBOLT ENTERPRISES
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
RICHBOLT ENTERPRISESFDA reg. 8043622SIALKOT Punjab, PakistanManufacturer

Sources

FDA establishment registration & device listing (search FDA, owner/operator 9002758). 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.