FDA Registration Active 🇸🇪 Sweden

STILLE AB

Reg #: 3003696170 · FEI: 3003696170 · Expires 2026
Products
39
Proprietary Names
4
Establishment Types
3
Classifications
39

Registration Details

Registration Name
STILLE AB
Registration Number
3003696170
FEI Number
3003696170
Status
Active
Expiry Year
2026
Initial Importer
No
Address
Ekbacken 11
City
Torshalla Sodermanland
Country
SE

Owner / Operator

Firm Name
STILLE AB
Operator Number
9036158
Address
Ekbacken 11, --
City
Torshalla
State
Sodermanland
Postal Code
SE-644 30
Country
SE

US Agent

Business Name
J & D CAMPBELL ASSOCIATES, INC.
Contact Name
JANE CAMPBELL
Address
164 HAMMOCK AVE
City
PAWLEYS ISLAND
State
SC
ZIP
29585
Country
US
Phone
843 3143670 ext. 0

Products

Device Name Product Code
Marker, Skin FZZ
Hemostat HRQ
Scissors, Ophthalmic HNF
Rongeur HTX
Curette HTF
Instrument, Surgical, Non-Powered HAO
Gouge, Surgical, General & Plastic Surgery GDH
Guide, Surgical, Instrument FZX
Bedding, Disposable, Medical KME
Speculum, Ent EPY
Curtain, Protective, Radiographic IWQ
Mallet HXL
Instrument, Cutting, Orthopedic HTZ
Scissors, Nasal KBD
Holder, Needle; Orthopedic HXK
Saw HSO
Instruments, Surgical, Cardiovascular DWS
Dissector, Surgical, General & Plastic Surgery GDI
Instrument, Bending Or Contouring HXP
Holder, Needle, Gastroenterologic FHQ
Handle, Scalpel GDZ
Scissors, Orthopedic, Surgical HRR
Chisel (Osteotome) KDG
Forceps, General & Plastic Surgery GEN
Table, Examination, Medical, Powered LGX
Knife, Orthopedic HTS
Table, Operating-Room, Electrical GDC
Cannula, Surgical, General & Plastic Surgery GEA
Rasp HTR
Probe HXB
Elevator HTE
Scoop FHL
Clamp, Surgical, General & Plastic Surgery GDJ
Retractor GAD
Instrument, Cast Application/Removal, Manual LGG
Stripper, Surgical HRT
Scissors, General, Surgical LRW
Forceps, Ent KAE
Saw, Nasal KBC

Proprietary Names

Disposable Covers 119-50015, ROUND GRIP SCALPEL HANDLE STILLE blade 10-15 14.5 cm 5.75 in 540-1200, GS2 Operation Table Stille imagiQ2

Establishment Types

Manufacture Medical Device Complaint File Establishment per 21 CFR 820.198 Repack or Relabel Medical Device